Risk of tumorigenesis in overgrowth syndromes: A comprehensive review

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

Pilia, G., Hughes-Benzie, R., MacKenzie, A., Baybayan, P. A., Chen, E. Y., Huber, R., Neri, G., Cao, A., Forabosco, A., & Schlessinger, D. (1996) · Nature Genetics · doi:10.1038/ng0396-241 · Cited by 750

Haploinsufficiency of NSD1 causes Sotos syndrome

Kurotaki, N., Imaizumi, K., Harada, N., Masuno, M., Kondoh, T., Nagai, T., Ohashi, H., Naritomi, K., Tsukahara, M., Makita, Y., et al. (2002) · Nature Genetics · doi:10.1038/ng863 · Cited by 647

PTEN Mutation Spectrum and Genotype-Phenotype Correlations in Bannayan-Riley-Ruvalcaba Syndrome Suggest a Single Entity With Cowden Syndrome

Marsh, D. J., Kum, J. B., Lunetta, K. L., Bennett, M. J., Gorlin, R. J., Ahmed, S. F., Bodurtha, J. N., Crowe, C. A., Curtis, M. A., Dasouki, M., et al. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.8.1461 · Cited by 609

Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry

DeBaun, M. R., & Tucker, M. A. (1998) · The Journal of Pediatrics · doi:10.1016/s0022-3476(98)70008-3 · Cited by 439

Clinical features and natural history of Beckwith‐Wiedemann syndrome: presentation of 74 new cases

Elliott, M. M., Bayly, R. J., Cole, T., Temple, I. K., & Maher, E. R. (1994) · Clinical Genetics · doi:10.1111/j.1399-0004.1994.tb04219.x · Cited by 423

Management of Genetic Syndromes

(2005) · Wiley eBooks · doi:10.1002/0471695998 · Cited by 392

An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome

Hatada, I., Ohashi, H., Fukushima, Y., Kaneko, Y., Inoue, M., Komoto, Y., Okada, A., Oh‐ishi, S., Nabetani, A., Morisaki, H., et al. (1996) · Nature Genetics · doi:10.1038/ng1096-171 · Cited by 382

Sotos syndrome: a study of the diagnostic criteria and natural history.

Cole, T. R. P., & Hughes, H. E. (1994) · Journal of Medical Genetics · doi:10.1136/jmg.31.1.20 · Cited by 314

Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects

Christensen, B., Arbour, L. T., Tran, P. V., Leclerc, D., Sabbaghian, N., Platt, R. W., Gilfix, B. M., Rosenblatt, D. S., Gravel, R. A., Forbes, P. A., et al. (1999) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19990521)84:2 · Cited by 305

NSD1 Mutations Are the Major Cause of Sotos Syndrome and Occur in Some Cases of Weaver Syndrome but Are Rare in Other Overgrowth Phenotypes

Douglas, J. B., Hanks, S., Temple, I. K., Davies, S. J., Murray, A., Upadhyaya, M., Tomkins, S. E., Hughes, H. E., Cole, R. P. T., & Rahman, N. (2003) · The American Journal of Human Genetics · doi:10.1086/345647 · Cited by 301

Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature

Pettenati, M. J., Haines, J. L., Higgins, R. R., Wappner, R. S., Palmer, C. G., & Weaver, D. D. (1986) · Human Genetics · doi:10.1007/bf00282078 · Cited by 300

A population-based case-control study of childhood leukemia in shanghai

Shu, X. O., Gao, Y. T., Tu, J., Zheng, W., Brinton, L. A., Linet, M. S., & Fraumeni, J. F. (1988) · Cancer · doi:10.1002/1097-0142(19880801)62:3 · Cited by 291

Complete and incomplete forms of Beckwith-Wiedemann syndrome: Their oncogenic potential

Sotelo‐Avila, C., Gonzalez‐Crussi, F., & Fowler, J. W. (1980) · The Journal of Pediatrics · doi:10.1016/s0022-3476(80)80322-2 · Cited by 290

Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development

Weksberg, R. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddg067 · Cited by 290

Tumours and hemihypertrophy associated with Wiedemann-Beckwith syndrome

Wiedemann, H. R. (1983) · European Journal of Pediatrics · doi:10.1007/bf00496807 · Cited by 281 · cited 1×

Epigenetic Alterations of H19 and LIT1 Distinguish Patients with Beckwith-Wiedemann Syndrome with Cancer and Birth Defects

DeBaun, M. R., Niemitz, E. L., McNeil, D. E., Brandenburg, S. A., Lee, M. P., & Feinberg, A. P. (2002) · The American Journal of Human Genetics · doi:10.1086/338934 · Cited by 275

Hereditary Gastrointestinal Polyposis Syndromes

Haggitt, R. C., & Reid, B. J. (1986) · The American Journal of Surgical Pathology · doi:10.1097/00000478-198612000-00006 · Cited by 271

Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1

Weksberg, R. (2001) · Human Molecular Genetics · doi:10.1093/hmg/10.26.2989 · Cited by 247

Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1

Lin, A. E., Birch, P. H., Korf, B. R., Tenconi, R., Niimura, M., Pöyhönen, M., Uhas, K. A., Sigorini, M., Virdis, R., Romano, C., et al. (2000) · American Journal of Medical Genetics · doi:10.1002/1096-8628(20001113)95:2 · Cited by 243

Reassessment of the Proteus syndrome literature: Application of diagnostic criteria to published cases

Turner, J. T., Cohen, M. M., & Biesecker, L. G. (2004) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.30327 · Cited by 237

Imprinting mutations in the Beckwith—Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2–H19 domain

Reik, W., Brown, K. W., Schneid, H., Bouc, Y. L., Bickmore, W. A., & Maher, E. R. (1995) · Human Molecular Genetics · doi:10.1093/hmg/4.12.2379 · Cited by 217

Beckwith-Wiedemann syndrome.

Elliott, M., & Maher, E. R. (1994) · Journal of Medical Genetics · doi:10.1136/jmg.31.7.560 · Cited by 187

Dysmyelopoietic syndromes a search for prognostic factors in 193 patients

Coiffier, B., Adeleine, P., Viala, J. J., Bryon, P. A., Fiere, D. M., Gentilhomme, O., & Vuvan, H. (2006) · Cancer · doi:10.1002/1097-0142(19830701)52:1 · Cited by 182

Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation

Lam, W. W. K., Hatada, I., Oh‐ishi, S., Mukai, T., Joyce, J. A., Cole, T. R. P., Donnai, D., Reik, W., Schofield, P. N., & Maher, E. R. (1999) · Journal of Medical Genetics · doi:10.1136/jmg.36.7.518 · Cited by 181

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

Engel, J. R., Smallwood, A., Harper, A., Higgins, M. J., Oshimura, M., Reik, W., Schofield, P. N., & Maher, E. R. (2000) · Journal of Medical Genetics · doi:10.1136/jmg.37.12.921 · Cited by 181

Hepatoblastoma

Lack, E. E., Neave, C., & Vawter, G. F. (1982) · The American Journal of Surgical Pathology · doi:10.1097/00000478-198212000-00001 · Cited by 179

Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS

Bliek, J. (2001) · Human Molecular Genetics · doi:10.1093/hmg/10.5.467 · Cited by 177

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith–Wiedemann syndrome

Gaston, V., Bouc, Y. L., Soupre, V., Bürglen, L., Donadieu, J., Oro, H., Audry, G., Vazquez, M., & Gicquel, C. (2001) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5200649 · Cited by 173

Adrenocortical neoplasms with hemihypertrophy, brain tumors, and other disorders

Fraumeni, J. F., & Miller, R. W. (1967) · The Journal of Pediatrics · doi:10.1016/s0022-3476(67)80179-3 · Cited by 169

Five additional Costello syndrome patients with rhabdomyosarcoma: Proposal for a tumor screening protocol

Gripp, K. W., Scott, C. I., Nicholson, L., McDonald‐McGinn, D. M., Ozeran, J. D., Jones, M. C., Lin, A. E., & Zackai, E. H. (2002) · American Journal of Medical Genetics · doi:10.1002/ajmg.10241 · Cited by 156

Isolated hemihyperplasia (hemihypertrophy): Report of a prospective multicenter study of the incidence of neoplasia and review

Hoyme, H. E., Seaver, L. H., Jones, K. L., Procopio, F., Crooks, W., & Feingold, M. (1998) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19981002)79:4 · Cited by 149

Screening for Wilms tumor in children with Beckwith-Wiedemann syndrome or idiopathic hemihypertrophy

Choyke, P. L., Siegel, M. J., Craft, A. W., Green, D. M., & DeBaun, M. R. (1999) · Medical and Pediatric Oncology · doi:10.1002/(sici)1096-911x(199903)32:3 · Cited by 148

Proteus syndrome: Clinical evidence for somatic mosaicism and selective review

Cohen, M. M. (1993) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320470514 · Cited by 147

Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma.

Henry, I., Grandjouan, S., Couillin, P., Barichard, F., Huerre-Jeanpierre, C., Glaser, T. M., Philip, T. O., Lenoir, G., Chaussain, J., & Junien, C. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.9.3247 · Cited by 144

Hypersensitive reactions and antibody formation during L-asparaginase treatment of children and adults with acute leukemia

Killander, D., Dohlwitz, A., Engstedt, L., Franzén, S., Gahrton, G., GULLBRING, B., Holm, G., Holmgren, A., Höglund, S., KILLANDER, A., et al. (1976) · Cancer · doi:10.1002/1097-0142(197601)37:1 · Cited by 143

Somatic Mosaicism for Partial Paternal Isodisomy in Wiedemann-Beckwith Syndrome: A Post-Fertilization Event

Henry, I., Puech, A., Riesewijk, A. M., Ahnine, L., Mannens, M. M. A. M., Beldjord, C., Bitoun, P., Tournade, M. F., Landrieu, P., & Junien, C. (1993) · European Journal of Human Genetics · doi:10.1159/000472384 · Cited by 141

WILMS' TUMOR AND CONGENITAL HEMIHYPERTROPHY: REPORT OF FIVE NEW CASES AND REVIEW OF LITERATURE

Fraumeni, J. F., Geiser, C. F., & Manning, M. D. (1967) · PEDIATRICS · doi:10.1542/peds.40.5.886 · Cited by 140

Inadequate corpus luteum function: A pathophysiological interpretation of human breast cancer epidemiology

Sherman, B. M., & Korenman, S. G. (1974) · Cancer · doi:10.1002/1097-0142(197405)33:5 · Cited by 140

A newly recognized hamartomatous syndrome.

Cohen, M. M., & Hayden, P. W. (1979) · PubMed · Cited by 138

Low Frequency of p57KIP2 Mutation in Beckwith-Wiedemann Syndrome

Lee, M. P., DeBaun, M. R., Randhawa, G. S., Reichard, B. A., Elledge, S. J., & Feinberg, A. P. (1997) · The American Journal of Human Genetics · doi:10.1086/514858 · Cited by 137

Coding Mutations in p57 Are Present in Some Cases of Beckwith-Wiedemann Syndrome but Are Rare or Absent in Wilms Tumors

O’Keefe, D., Dao, D., Zhao, L., Sanderson, R., Warburton, D., Weiss, L. M., Anyane‐Yeboa, K., & Tycko, B. (1997) · The American Journal of Human Genetics · doi:10.1086/514854 · Cited by 135

Spectrum of NSD1 mutations in Sotos and Weaver syndromes

Rio, M., Clech, L., Amiel, J., Faivre, L. O., Lyonnet, S., Merrer, M. F. L., Odent, S., Lacombe, D., Edery, P., Brauner, R., et al. (2003) · Journal of Medical Genetics · doi:10.1136/jmg.40.6.436 · Cited by 134

Descriptive analysis of tibial pseudarthrosis in patients with neurofibromatosis 1

Stevenson, D. A., Birch, P. H., Friedman, J. M., Viskochil, D. H., Balestrazzi, P., Boni, S., Buske, A., Korf, B. R., Niimura, M., Pivnick, E. K., et al. (1999) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19990611)84:5 · Cited by 130

Macrocephaly with cutis marmorata, haemangioma and syndactyly ??? a distinctive overgrowth syndrome

Clayton‐Smith, J., Kerr, B. A., Brunner, H. G., Tranebjærg, L., Magee, A. J., Hennekam, R. C. M., Mueller, R. F., Brueton, L. A., Super, M., Steen-Johnsen, J., et al. (1997) · Clinical Dysmorphology · doi:10.1097/00019605-199710000-00001 · Cited by 127

GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome

Li, M., Shuman, C. T., Fei, Y. L., Cutiongco, E. M., Bender, H. A., Stevens, C. A., Wilkins-Haug, L. E., Day-Salvatore, D.-L., Yong, S. L., Geraghty, M. T., et al. (2001) · American Journal of Medical Genetics · doi:10.1002/1096-8628(20010801)102:2 · Cited by 126

Deletions of 20p12 in Alagille syndrome: Frequency and molecular characterization

Krantz, I. D., Rand, E. B., Genin, A., Hunt, P., Jones, M. C., Louis, A. A., Graham, J. M., Bhatt, S., Piccoli, D. A., & Spinner, N. B. (1997) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19970502)70:1 · Cited by 117

Overgrowth Syndromes

Cohen, M. M., Neri, G., & Weksberg, R. (2001) · Cited by 117

A Comprehensive and Critical Assessment of Overgrowth and Overgrowth Syndromes

Cohen, M. M. (1989) · Springer eBooks · doi:10.1007/978-1-4613-0785-3_4 · Cited by 115

CNS late effects after ALL therapy in childhood. Part I: Neuroradiological findings in long-term survivors of childhood ALL—an evaluation of the interferences between morphology and neuropsychological performance

Hertzberg, H., Huk, W. J., Ueberall, M. A., Langer, T., Meier, W., Dopfer, R. E., Skalej, M., Lackner, H., Bode, U., Janßen, G., et al. (1997) · Medical and Pediatric Oncology · doi:10.1002/(sici)1096-911x(199706)28:6 · Cited by 111

Neoplasms associated with the Beckwith-Wiedemann syndrome.

Sotelo‐Avila, C., & Gooch, W. M. (1976) · PubMed · Cited by 111

Screening of children with hemihypertrophy, aniridia, and Beckwith‐Wiedemann syndrome in patients with wilms tumor: A report from the national Wilms tumor study

Green, D. M., Breslow, N. E., Beckwith, J. B., & Norkool, P. A. (1993) · Medical and Pediatric Oncology · doi:10.1002/mpo.2950210307 · Cited by 109

Risk of malignancy in Sotos syndrome

Hersh, J. H., Cole, T. R. P., Bloom, A. S., Bertolone, S. J., & Hughes, H. E. (1992) · The Journal of Pediatrics · doi:10.1016/s0022-3476(10)80004-6 · Cited by 103

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma

Henry, I., Jeanpierre, M., Couillin, P., Barichard, F., Serre, J., Journel, H., Lamouroux, A., TURLEAU, C., GROUCHY, J. D., & Junien, C. (1989) · Human Genetics · doi:10.1007/bf00279003 · Cited by 100

The Multifaceted Challenges of Proteus Syndrome

Biesecker, L. G. (2001) · JAMA · doi:10.1001/jama.285.17.2240 · Cited by 100

Congenital Pancreatoblastoma in Beckwith Wiedemann Syndrome

Drut, R., & Jones, M. C. (1988) · Pediatric Pathology · doi:10.3109/15513818809042976 · Cited by 100

Serum α-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasia

Clericuzio, C. L., Chen, E., McNeil, D. E., O'Connor, T., Zackai, E. H., Medne, L., Tomlinson, G. E., & DeBaun, M. R. (2003) · The Journal of Pediatrics · doi:10.1067/s0022-3476(03)00306-8 · Cited by 99

Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS)

Bliek, J., Gicquel, C., Maas, S. M., Gaston, V., Bouc, Y. L., & Mannens, M. M. A. M. (2004) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2004.08.007 · Cited by 99

Macrocephaly‐cutis marmorata telangiectatica congenita: Report of six new patients and a review

Lapunzina, P. D., Gairí, A., Delicado, A., Mori, M. A., Torres, M. L., Goma, A., Navia, M., & Pajares, I. L. (2004) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.30235 · Cited by 99

Characteristics and Outcome of Children With Beckwith-Wiedemann Syndrome and Wilms’ Tumor: A Report From the National Wilms Tumor Study Group

Porteus, M. H., Narkool, P., Neuberg, D. S., Guthrie, K. A., Breslow, N. E., Green, D. M., & Diller, L. (2000) · Journal of Clinical Oncology · doi:10.1200/jco.2000.18.10.2026 · Cited by 96

Syndrome of accelerated skeletal maturation and relative failure to thrive: A newly recognized clinical growth disorder

Marshall, R. E., Graham, C. B., Scott, C. R., & Smith, D. W. (1971) · The Journal of Pediatrics · doi:10.1016/s0022-3476(71)80269-x · Cited by 96

Longitudinal observations on 15 children with Wiedemann‐Beckwith syndrome

Weng, E. Y., Moeschler, J. B., & Graham, J. M. (1995) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320560405 · Cited by 96

Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.

Slatter, R., Elliott, M. M., Welham, K., Carrera, M., Schofield, P. N., Barton, D. E., & Maher, E. R. (1994) · Journal of Medical Genetics · doi:10.1136/jmg.31.10.749 · Cited by 95

New p57 KIP2 mutations in Beckwith-Wiedemann syndrome

Hatada, I., Nabetani, A., Morisaki, H., Xin, Z., Ohishi, S., Tonoki, H., Niikawa, N., Inoue, M., Komoto, Y., Okada, A., et al. (1997) · Human Genetics · doi:10.1007/s004390050573 · Cited by 94

Congenital anomalies associated with rhabdomyosarcoma: An autopsy study of 115 cases. A report from the intergroup rhabdomyosarcoma study committee (representing the children's cancer study group, the pediatric oncology group, the United Kingdom children's cancer study group, and the pediatric intergroup statistical center)

Ruymann, F. B., Maddux, H. R., Ragab, A. H., Soule, E. H., Palmer, N., Beltangady, M. S., Gehan, E. A., & Newton, W. A. (1988) · Medical and Pediatric Oncology · doi:10.1002/mpo.2950160109 · Cited by 91

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.

Catchpoole, D. R., Lam, W. W. K., Valler, D., Temple, I. K., Joyce, J. A., Reik, W., Schofield, P. N., & Maher, E. R. (1997) · Journal of Medical Genetics · doi:10.1136/jmg.34.5.353 · Cited by 90

Neoplasms in proteus syndrome

Gordon, P., Wilroy, R. S., Lasater, O. E., & Michael, M. C. (1995) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320570117 · Cited by 89

Simpson Golabi Behmel Syndrome: Progress toward Understanding the Molecular Basis for Overgrowth, Malformation, and Cancer Predisposition

DeBaun, M. R., Ess, J., & Saunders, S. (2001) · Molecular Genetics and Metabolism · doi:10.1006/mgme.2001.3150 · Cited by 88

Systemic leishmaniasis mimicking malignant histiocytosis

Matzner, Y., Behar, A. J., Beery, E., Gunders, A. E., & Hershko, C. (1979) · Cancer · doi:10.1002/1097-0142(197901)43:1 · Cited by 86

Renal hamartomas and nephroblastomatosis with fetal gigantism: A familial syndrome

Perlman, M., Goldberg, G. M., Bar‐Ziv, J., & Danovitch, G. M. (1973) · The Journal of Pediatrics · doi:10.1016/s0022-3476(73)80264-1 · Cited by 86

Down Syndrome

(2002) · Wiley eBooks · doi:10.1002/0471227579 · Cited by 84

Cerebral gigantism (Sotos syndrome). Compiled data of 22 cases

Wit, J. M., Beemer, F. A., Barth, P. G., Oorthuys, J. W. E., Dijkstra, P. F., den Brande, J. L. V., & Leschot, N. J. (1985) · European Journal of Pediatrics · doi:10.1007/bf00451898 · Cited by 84

Cerebral gigantism: Endocrinological and clinical observations of six patients including a congenital giant, concordant monozygotic twins, and a child who achieved adult gigantic size

Hook, E. B., & Reynolds, J. W. (1967) · The Journal of Pediatrics · doi:10.1016/s0022-3476(67)80263-4 · Cited by 81

GPC4,the Gene for Human K-Glypican, FlanksGPC3on Xq26: Deletion of theGPC3–GPC4Gene Cluster in One Family with Simpson–Golabi–Behmel Syndrome

Veugelers, M., Vermeesch, J. R., Watanabe, K., Yamaguchi, Y., Marynen, P., & David, G. (1998) · Genomics · doi:10.1006/geno.1998.5465 · Cited by 80

Vasculogenesis, angiogenesis, hemangiomas, and vascular malformations

Cohen, M. M. (2002) · American Journal of Medical Genetics · doi:10.1002/ajmg.10260 · Cited by 79

Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome.

Schneid, H., Seurin, D., Vazquez, M., Gourmelen, M., Cabrol, S., & Bouc, Y. L. (1993) · Journal of Medical Genetics · doi:10.1136/jmg.30.5.353 · Cited by 78

Serum α-fetoprotein levels in Beckwith-Wiedemann syndrome

Everman, D. B., Shuman, C. T., Dzolganovski, B., O’Riordan, M. A., Weksberg, R., & Robin, N. H. (2000) · The Journal of Pediatrics · doi:10.1067/mpd.2000.106217 · Cited by 76

Congenital hemihypertrophy

Gorlin, R. J., & Meskin, L. H. (1962) · The Journal of Pediatrics · doi:10.1016/s0022-3476(62)80198-x · Cited by 72

Perlman syndrome: Familial renal dysplasia with wilms tumor, fetal gigantism, and multiple congenital anomalies

Perlman, M., Opitz, J. M., & Reynolds, J. F. (1986) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320250418 · Cited by 72

Therapy for non-Hodgkin lymphoma in children with primary immunodeficiency: Analysis of 19 patients from the BFM trials

Seidemann, K., Tiemann, M., Henze, G., Sauerbrey, A., M�ller, S., & Reiter, A. (1999) · Medical and Pediatric Oncology · doi:10.1002/(sici)1096-911x(199912)33:6 · Cited by 70

CONGENITAL ASYMMETRY: REPORT OF 10 CASES WITH ASSOCIATED DEVELOPMENTAL ABNORMALITIES

Parker, D. A., & Skalko, R. G. (1969) · PEDIATRICS · doi:10.1542/peds.44.4.584 · Cited by 69

Klippel-Trenaunay Syndrome Associated with Urinary Tract Hemangiomas

Klein, T., & Kaplan, G. W. (1975) · The Journal of Urology · doi:10.1016/s0022-5347(17)67092-7 · Cited by 69

Understanding Proteus syndrome, unmasking the elephant man, and stemming elephant fever.

Mm, C. (1988) · PubMed · Cited by 68

Wilms's Tumor in Three Children of a Woman with Congenital Hemihypertrophy

Meadows, A. T., Lichtenfeld, J. L., & Koop, C. E. (1974) · New England Journal of Medicine · doi:10.1056/nejm197407042910106 · Cited by 66

The Perlman syndrome: Familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies

Neri, G., Martini‐Neri, M. E., Katz, B. E., & Opitz, J. M. (1984) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320190120 · Cited by 65

Favorable outcome in children with Beckwith-Wiedeman syndrome and intraabdominal malignant tumors

Vaughan, W. G., Sanders, D., Grosfeld, J. L., Plumley, D. A., Rescorla, F. J., Scherer, L. R., West, K. W., & Breitfeld, P. P. (1995) · Journal of Pediatric Surgery · doi:10.1016/0022-3468(95)90338-0 · Cited by 64

The Perlman familial nephroblastomatosis syndrome

Greenberg, F., Stein, F., Gresik, M. V., Finegold, M. J., Carpenter, R. J., Riccardi, V. M., Beaudet, A. L., Opitz, J. M., & Reynolds, J. F. (1986) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320240112 · Cited by 64

Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

Lindsay, S., Ireland, M., O’Brien, O., Clayton‐Smith, J., Hurst, J. A., Mann, J., Cole, T. J., Sampson, J., Slaney, S. F., Schlessinger, D., et al. (1997) · Journal of Medical Genetics · doi:10.1136/jmg.34.6.480 · Cited by 64

Orthotopic liver transplantation for unresectable hepatoblastoma: A single center's experience

Al-Oabandi, W., Jenkinson, H. C., BUCKELS, J. A. C., Mayer, A. D., McKiernan, P. J., Morland, B. J., John, P., & Kelly, D. A. (1999) · Journal of Pediatric Surgery · doi:10.1016/s0022-3468(99)90164-1 · Cited by 63

Association of Alveolar Rhabdomyosarcoma with the Beckwith-Wiedemann Syndrome

Smith, A. C., Squire, J. A., Thorner, P. S., Zieleńska, M., Shuman, C. T., Grant, R. M., Chitayat, D. A., Nishikawa, J. L., & Weksberg, R. (2001) · Pediatric and Developmental Pathology · doi:10.1007/s10024001-0110-6 · Cited by 60

Proteus syndrome: Misdiagnosis with PTEN mutations

M. Michael Cohen, Turner, J. T., & Biesecker, L. G. (2003) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.20474 · Cited by 60

Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome

Little, M. H., Thomson, D. B., Hayward, N. K., & Smith, P. J. (1988) · Human Genetics · doi:10.1007/bf00280564 · Cited by 59

Loss of Imprinting of Human Insulin-like Growth Factor II Gene, IGF2, in Acute Myeloid Leukemia

Wu, H., Weksberg, R., Minden, M. D., & Squire, J. A. (1997) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.6127 · Cited by 56

Screening for wilms' tumour in patients with aniridia, Beckwith syndrome, or hemihypertrophy

Craft, A. W., Parker, L., Stiller, C. A., & Cole, M. F. (1995) · Medical and Pediatric Oncology · doi:10.1002/mpo.2950240404 · Cited by 56

Inherited Disorders of the Skeleton

Young, I. D. (1989) · Journal of Medical Genetics · doi:10.1136/jmg.26.5.350-a · Cited by 54

Prophylaxis of varicella in children with neoplastic disease: Comparative results with zoster immune plasma and gamma globulin

Geiser, C. F., Bishop, Y. M. M., Myers, M., Jaffe, N., & Yankee, R. A. (1975) · Cancer · doi:10.1002/1097-0142(197504)35:4 · Cited by 54

Hereditary febrile seizures: Phenotype and evidence for a chromosome 19p locus

Kugler, S. L., Stenroos, E. S., Mandelbaum, D. E., Lehner, T., McKoy, V. V., Prossick, T., Sasvari, J., Swannick, K., Katz, J., & Johnson, W. G. (1998) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19981012)79:5 · Cited by 54

Linkage study of the α2A adrenergic receptor in attention-deficit hyperactivity disorder families

Xu, C., Schachar, R. J., Tannock, R., Roberts, W., MALONE, M. A., Kennedy, J. L., & Barr, C. L. (2001) · American Journal of Medical Genetics · doi:10.1002/1096-8628(2001)9999:9999 · Cited by 53

Perlman and Wiedemann-Beckwith syndromes: Two distinct conditions associated with Wilms' tumour

Grundy, R. G., Pritchard, J., Baraitser, M., Risdon, A., & Robards, M. (1992) · European Journal of Pediatrics · doi:10.1007/bf01954125 · Cited by 53

Expanding the spectrum of the Perlman syndrome

Greenberg, F., Copeland, K., Gresik, M. V., Optiz, J. M., & Reynolds, J. F. (1988) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320290406 · Cited by 53

Pancreatoblastoma in a neonate with Wiedemann-Beckwith syndrome

Koh, T. H. H. G., Cooper, J. E., Newman, C. L., Walker, T. M., Kiely, E. M., & Hoffmann, E. B. (1986) · European Journal of Pediatrics · doi:10.1007/bf00439255 · Cited by 52

EPITHELIAL HEPATOBLASTOMA ASSOCIATED WITH CONGENITAL HEMIHYPERTROPHY AND CYSTATHIONINURIA: PRESENTATION OF A CASE

Geiser, C. F., Baez, A., Am, S., & Shih, V. E. (1970) · PEDIATRICS · doi:10.1542/peds.46.1.66 · Cited by 50

Clinical overlap of Beckwith‐Wiedemann, Perlman and Simpson‐Golabi‐Behmel syndromes: a diagnostic pitfall

Verloès, A., Massart, B., Dehalleux, I., Langhendries, J., & Koulischer, L. (1995) · Clinical Genetics · doi:10.1111/j.1399-0004.1995.tb04307.x · Cited by 49

A patient with Simpson-Golabi-Behmel syndrome and hepatocellular carcinoma.

Lapunzina, P. D., Badia, I. B., Galoppo, C., Matteo, E. D., Silberman, P., Tello, A., Grichener, J., & Hughes-Benzie, R. (1998) · Journal of Medical Genetics · doi:10.1136/jmg.35.2.153 · Cited by 49

Compromise of the spinal canal in Proteus syndrome

Skovby, F., Graham, J. M., Sonne‐Holm, S., & Cohen, M. M. (1993) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320470516 · Cited by 47

Linear nevi, hemihypertrophy, connective tissue hamartomas, and unusual neoplasms in children

Hornstein, L., Bove, K. E., & Towbin, R. B. (1987) · The Journal of Pediatrics · doi:10.1016/s0022-3476(87)80502-4 · Cited by 44

Wilms Tumor Screening Is Unnecessary in Klippel-Trenaunay Syndrome

Greene, A. K., Kieran, M. W., Burrows, P. E., Mulliken, J. B., Kasser, J. R., & Fishman, S. J. (2004) · PEDIATRICS · doi:10.1542/peds.113.4.e326 · Cited by 44

Beckwith-Wiedemann syndrome: Role of ultrasound in its management

Shah, K. J. (1983) · Clinical Radiology · doi:10.1016/s0009-9260(83)80346-8 · Cited by 43

Neoplasms Associated With Hemihypertrophy, Beckwith-Wiedemann Syndrome and Aniridia

Tank, E. S., & Kay, R. (1980) · The Journal of Urology · doi:10.1016/s0022-5347(17)55401-4 · Cited by 43

Ophthalmologic Examinadon in the Diagnosis of Proteus Syndrome

Bouzas, E. A., Krasnewich, D., Koutroumanidis, M., Papadimitriou, A., Marini, J. C., & Kaiser‐Kupfer, M. I. (1993) · Ophthalmology · doi:10.1016/s0161-6420(93)31645-3 · Cited by 42

RENAL FINDINGS ON RADIOLOGICAL FOLLOWUP OF PATIENTS WITH BECKWITH-WIEDEMANN SYNDROME

Borer, J. G., Kaefer, M. A., Barnewolt, C. E., Elias, E. R., Hobbs, N., RETIC, A. B., & Peters, C. A. (1999) · The Journal of Urology · doi:10.1016/s0022-5347(01)62118-9 · Cited by 42

Marshall–Smith syndrome: Natural history and evidence of an osteochondrodysplasia with connective tissue abnormalities

Adam, M. P., Hennekam, R. C. M., Keppen, L. D., Bull, M. J., Clericuzio, C. L., Burke, L. W., Ormond, K. E., & Hoyme, H. E. (2005) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.30580 · Cited by 42

Proteus syndrome: Course of a severe case

Malamitsi‐Puchner, A., Dimitriadis, D., Bartsocas, C. S., & Wiedemann, H. ‐. (1990) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320350228 · Cited by 41

Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma

Haas, O. A., Zoubek, A., Grümayer, E. R., & Gadner, H. (1986) · Cancer Genetics and Cytogenetics · doi:10.1016/0165-4608(86)90409-7 · Cited by 40

Cerebral Gigantism Associated With Wilms' Tumor

Maldonado, V. (1984) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/archpedi.1984.02140430062016 · Cited by 39

Beckwith-Wiedemann Syndrome-associated Hepatoblastoma: Wnt Signal Activation Occurs Later in Tumorigenesis in Patients with 11p15.5 Uniparental Disomy

Fukuzawa, R., Hata, J., Hayashi, Y., Ikeda, H., & Reeve, A. E. (2003) · Pediatric and Developmental Pathology · doi:10.1007/s10024-003-1009-1 · Cited by 39

Genome-wide loss of maternal alleles in a nephrogenic rest and Wilms' tumour from a BWS patient

Hoban, P. R., Heighway, J., White, G. M., Baker, B., Gardner, J., Birch, J., Morris-Jones, P., & Kelsey, A. M. (1995) · Human Genetics · doi:10.1007/bf00209482 · Cited by 38

Neodymium: Yag laser irradiation of bladder hemangioma

Smith, J. A. J., & Dixon, J. A. (1984) · Urology · doi:10.1016/0090-4295(84)90414-x · Cited by 38

Periconceptional intake of vitamin supplements and risk of multiple congenital anomalies

Shaw, G. M., Croen, L., Todoroff, K., & Tolarová, M. M. (2000) · American Journal of Medical Genetics · doi:10.1002/1096-8628(20000731)93:3 · Cited by 36

The cutaneous manifestations of the Klippel-Trenaunay-Weber syndrome

Viljoen, D. L., Saxe, N., PEARNJ, J., & Beighton, P. (1987) · Clinical and Experimental Dermatology · doi:10.1111/j.1365-2230.1987.tb01845.x · Cited by 35

Neuroblastoma in a patient with Sotos' syndrome.

NANCE, M. A., Neglia, J. P., Talwar, D., & Berry, S. A. (1990) · Journal of Medical Genetics · doi:10.1136/jmg.27.2.130 · Cited by 35

Recognition and management of childhood cancer syndromes: A systems approach

Clericuzio, C. L. (1999) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19990625)89:2 · Cited by 34

Wilms' tumor in a patient with Beckwith-Wiedemann syndrome: onset detected with 3-month serial sonography.

Andrews, M., & Amparo, E. G. (1993) · American Journal of Roentgenology · doi:10.2214/ajr.160.1.8380110 · Cited by 34

Bladder Hemangiomas in Klippel-Trenaunay-Weber Syndrome

Hall, B. D. (1971) · New England Journal of Medicine · doi:10.1056/nejm197110282851816 · Cited by 34

Generation of homozygosity at the c-Ha-ras-1 locus on chromosome 11p in an adrenal adenoma from an adult with Wiedemann—Beckwith syndrome

Hayward, N. K., Little, M. H., Mortimer, R. H., Clouston, W. M., & Smith, P. J. (1988) · Cancer Genetics and Cytogenetics · doi:10.1016/0165-4608(88)90100-8 · Cited by 33

A Case of Cerebral Gigantism and Hepatocarcinoma

Sugarman, G. I. (1977) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/archpedi.1977.02120190025004 · Cited by 33

Congenital Asymmetry (Hemihypertrophy) and Abdominal Disease

Pfister, R. C., Weber, A. L., Smith, E. H., Wilkinson, R. H., & May, D. A. (1975) · Radiology · doi:10.1148/116.3.685 · Cited by 33

RADIOLOGY OF THE BECKWITH-WIEDEMANN SYNDROME

Lee, F. A. (1972) · Radiologic Clinics of North America · doi:10.1016/s0033-8389(22)01949-2 · Cited by 33

Hepatoblastoma associated with Beckwith-Wiedemann syndrome and hemihypertrophy

Hamada, Y., Takada, K., Fukunaga, S., & Hioki, K. (2003) · Pediatric Surgery International · doi:10.1007/s00383-002-0734-2 · Cited by 32

Beckwith-Wiedemann syndrome. Wilms' tumor, cardiac hamartoma, persistent visceromegaly, and glomeruloneogenesis in a 2-year-old boy.

Jk, R., Rn, S., Chang, C. H., Svoboda, D. J., Slaven, J., & Therou, L. (1972) · PubMed · Cited by 32

Demonstration of both primary and secondary reninism in renal tumors in children

Yokomori, K., Hori, T., Takemura, T., & Tsuchida, Y. (1988) · Journal of Pediatric Surgery · doi:10.1016/s0022-3468(88)80435-4 · Cited by 32

Congenital hemihypertrophy with adrenal adenoma and medullary sponge kidney

Tomooka, Y., Onitsuka, H., Goya, T., Hayashida, Y., Kuroiwa, T., Kudo, S., Miyazaki, S., & Torisu, M. (1988) · British Journal of Radiology · doi:10.1259/0007-1285-61-729-851 · Cited by 32

Wilms' tumor and adrenocortical carcinoma with hemihypertrophy and hamartomas

Mller, S., Gadner, H., Weber, B., Vogel, M., & Riehm, H. (1978) · European Journal of Pediatrics · doi:10.1007/bf00442064 · Cited by 32

Antenatal manifestation of congenital pancreatoblastoma in a fetus with Beckwith–Wiedemann syndrome

Pelizzo, G., Conoscenti, G., Kalache, K. D., Vesce, F., Guerrini, P., & Cavazzini, L. (2003) · Prenatal Diagnosis · doi:10.1002/pd.575 · Cited by 32

Beckwith-Wiedemann syndrome. Clinical comparison between patients with and without 11p15 trisomy.

TURLEAU, C., & GROUCHY, J. D. (1985) · PubMed · Cited by 32

Small cell lung carcinoma in a patient with Sotos syndrome: are genes at 3p21 involved in both conditions?

Cole, T. R. P., Hughes, H. E., Jeffreys, M. J., Williams, G. T., & Arnold, M. M. (1992) · Journal of Medical Genetics · doi:10.1136/jmg.29.5.338 · Cited by 31

Extending the overlap of three congenital overgrowth syndromes

Coppin, B., Moore, I. E., & Hatchwell, E. (1997) · Clinical Genetics · doi:10.1111/j.1399-0004.1997.tb02494.x · Cited by 31

Patient with large 17p11.2 deletion presenting with Smith-Magenis syndrome and Joubert syndrome phenotype

Natacci, F., Corrado, L., Pierri, M., Rossetti, M., Zuccarini, C., Riva, P., Miozzo, M. R., & Larizza, L. (2000) · American Journal of Medical Genetics · doi:10.1002/1096-8628(20001218)95:5 · Cited by 30

Perlman syndrome: a case report emphasizing its similarity to and distinction from Beckwith-Wiedemann and prune-belly syndromes

Fahmy, J. L., Kaminsky, C. K., & Parisi, M. T. (1998) · Pediatric Radiology · doi:10.1007/s002470050326 · Cited by 30

Beckwith-wiedemann syndrome and neural crest tumors

Sirinelli, D., Silberman, B., Baudon, J.-J., Sinnassamy, P., Gruner, M., & Montagne, J. P. (1989) · Pediatric Radiology · doi:10.1007/bf02386843 · Cited by 30

Genital Tract Tumors in Proteus Syndrome: Report of a Case of Bilateral Paraovarian Endometrioid Cystic Tumors of Borderline Malignancy and Review of the Literature

Raju, R. R., Hart, W. R., Magnuson, D. K., Reid, J. R., & Rogers, D. G. (2002) · Modern Pathology · doi:10.1038/modpathol.3880510 · Cited by 29

Overgrowth

Sotos, J. F. (1997) · Clinical Pediatrics · doi:10.1177/000992289703600206 · Cited by 29

Beckwith-Wiedemann syndrome: Development of nephroblastoma during the surveillance period

Azouz, E. M., Larson, E. J., Patel, J., & Gyepes, M. T. (1990) · Pediatric Radiology · doi:10.1007/bf02011388 · Cited by 28

Perlman syndrome—a cause of enlarged, hyperechogenic kidneys

Chitty, L. S., Clark, T. J., & Maxwell, D. J. (1998) · Prenatal Diagnosis · doi:10.1002/(sici)1097-0223(199811)18:11 · Cited by 27

Cancer of the corpus uteri in white and black women in Michigan, 1985-1994

Madison, T., Schottenfeld, D., & Baker, V. M. (1998) · Cancer · doi:10.1002/(sici)1097-0142(19981015)83:8 · Cited by 27

Weaver syndrome and instability of the upper cervical spine

Muhonen, M. G., & Menezes, A. H. (1990) · The Journal of Pediatrics · doi:10.1016/s0022-3476(05)81611-7 · Cited by 27

Risks of congenital anomalies in large for gestational age infants

Lapunzina, P. D., López‐Camelo, J. S., Rittler, M., & Castilla, E. E. (2002) · The Journal of Pediatrics · doi:10.1067/mpd.2002.121696 · Cited by 27

Opsoclonus-myoclonus with Beckwith-Wiedemann syndrome and hepatoblastoma

Wilfong, A. A., Parke, J. T., & McCrary, J. A. (1992) · Pediatric Neurology · doi:10.1016/0887-8994(92)90060-c · Cited by 25

Section IV Genetic Disorders Associated with Overgrowth

Sotos, J. F. (1997) · Clinical Pediatrics · doi:10.1177/000992289703600106 · Cited by 25

High-resolution studies in patients with aniridia-Wilms tumor association, Wilms tumor or related congenital abnormalities

Nakagome, Y., Ise, T., Sakurai, M., Nakajo, T., Okamoto, E., Takano, T., Nakahori, Y., Tsuchida, Y., Nagahara, N., Takada, Y., et al. (1984) · Human Genetics · doi:10.1007/bf00291349 · Cited by 25

Computed Tomography and Ultrasound Findings in Klippel-Trenaunay Syndrome

Jafri, S. Z. H., Bree, R. L., Glazer, G. M., Francis, I. R., & Schwab, R. E. (1983) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-198306000-00014 · Cited by 25

Cancer in Sotos Syndrome: Report of a Patient With Acute Myelocytic Leukemia and Review of the Literature

Al-Mulla, N. A., Belgaumi, A., & Teebi, A. S. (2004) · Journal of Pediatric Hematology/Oncology · doi:10.1097/00043426-200403000-00013 · Cited by 25

Congenital Genitourinary Hemangiomas in a Patient with the Klippel-Trenaunay Syndrome: Management with the Neodymium:Yag Laser

Hockley, N. M., Bihrle, R., Bennett, R. M., & Curry, J. M. (1989) · The Journal of Urology · doi:10.1016/s0022-5347(17)41061-5 · Cited by 24

Congenital hemihypertrophy and associated abdominal lesions

Hennessy, W. T., Cromie, W. J., & Duckett, J. W. (1981) · Urology · doi:10.1016/0090-4295(81)90459-3 · Cited by 24

VIRILIZING ADRENAL ADENOMA IN AN ADULT WITH THE BECKWITH‐WIEDEMANN SYNDROME: PARADOXICAL RESPONSE TO DEXAMETHASONE

Clouston, W. M., Cannell, G. R., Fryar, B. G., Searle, J. W., MARTIN, N. I., & Mortimer, R. H. (1989) · Clinical Endocrinology · doi:10.1111/j.1365-2265.1989.tb01270.x · Cited by 24

Congenital Hepatoblastoma and Beckwith-Wiedemann Syndrome: A Case Study Including DNA Ploidy Profiles of Tumor and Adrenal Cytomegaly

Orozco, R., McBride, J. A., Favara, B. E., Steele, A., Brown, J., & Steele, P. (1991) · Pediatric Pathology · doi:10.3109/15513819109064749 · Cited by 24

Successful laparoscopic operation of bilateral pheochromocytoma in a patient with Beckwith-Wiedemann syndrome

Bémurat, L., Gosse, P., Ballanger, P., Tauzin-Fin, P., Barat, P., Lacombe, D., Lemétayer, P., & Clémenty, J. (2002) · Journal of Human Hypertension · doi:10.1038/sj.jhh.1001378 · Cited by 24

Neuroblastoma in a child with Wiedemann–Beckwith syndrome

Chitayat, D. A., Friedman, J. M., & Dimmick, J. E. (1990) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320350322 · Cited by 23

The Marshall-Smith syndrome: a review of the laryngeal complications

Cullen, A., Clarke, T. A., & O’Dwyer, T. P. (1997) · European Journal of Pediatrics · doi:10.1007/s004310050640 · Cited by 23

Adrenocortical carcinoma and congenital hemihypertrophy

Haicken, B. N., Schulman, N. H., & Schneider, K. M. (1973) · The Journal of Pediatrics · doi:10.1016/s0022-3476(73)80494-9 · Cited by 22

Successful airway control with the laryngeal mask in an infant with Beckwith–Wiedemann syndrome and hepatoblastoma for central line catheterization

Goldman, L. J., Nodal, C., & Jimenez, E. (2000) · Pediatric Anesthesia · doi:10.1046/j.1460-9592.2000.00548.x · Cited by 22

Lymphangiolipoma of the thoracic spine in a pediatric patient with Proteus syndrome

Whitley, J. M., & Flannery, A. M. (1996) · Child s Nervous System · doi:10.1007/bf00301256 · Cited by 22

Treatment strategy for nodular renal blastema and nephroblatomatosis associated with Wilms' tumor

Kumar, A., Pratt, C. B., Coburn, T. P., & Johnson, W. W. (1978) · Journal of Pediatric Surgery · doi:10.1016/s0022-3468(78)80401-1 · Cited by 22

Bilateral cystic adrenal masses in the neonate associated with the incomplete form of Beckwith-Wiedemann syndrome

Akata, D., Haliloğlu, M., Ozmen, M. N., & Akhan, O. (1997) · Pediatric Radiology · doi:10.1007/s002470050049 · Cited by 22

Atypical macrocephaly-cutis marmorata telangiectatica congenita with retinoblastoma

Schwartz, I. V. D., Felix, T. M. M., Riegel, M., & Schüler‐Faccini, L. (2002) · Clinical Dysmorphology · doi:10.1097/00019605-200207000-00010 · Cited by 22

Adrenocortical Tumors in Children: A Report of 12 Cases

Federici, S., Galli, G., Ceccarelli, P. L., Ferrari, M., Cicognani, A., CACCIARI, E., & Dòmini, R. (1994) · European Journal of Pediatric Surgery · doi:10.1055/s-2008-1066060 · Cited by 22

Wilms' Tumor Prior to Onset of Hemihypertrophy

Boxer, L. A. (1970) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/archpedi.1970.02100110112018 · Cited by 22

Hemangioma of the Bladder: Sonographic and Computerized Tomography Findings

Pakter, R. L., Nussbaum, A. R., & Fishman, E. K. (1988) · The Journal of Urology · doi:10.1016/s0022-5347(17)41732-0 · Cited by 22

Marshall-Smith syndrome

Summers, D. A., Cooper, H. A., & Butler, M. G. (1999) · Clinical Dysmorphology · doi:10.1097/00019605-199907000-00010 · Cited by 21

Is p57KIP2 mutation a common mechanism for Beckwith-Wiedemann syndrome or somatic overgrowth?

Okamoto, K., Morison, I. M., Reeve, A. E., Tommerup, N., Wiedemann, H. ‐., & Friedrich, U. (1998) · Journal of Medical Genetics · doi:10.1136/jmg.35.1.86 · Cited by 21

Lymphoproliferative disorders in Sotos syndrome: Observation of two cases

Corsello, G., Giuffrè, M., Carcione, A., Cuzto, M. L., Piccione, M., & Ziino, O. (1996) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19960906)64:4 · Cited by 20

Congenital hemihypertrophy and epithelioid haemangioendothelioma in a 10-year-old boy: a case report

Miller, J. H., Gillet, P. M., Hendry, G. M. A., & Wallace, W. H. (1999) · Pediatric Radiology · doi:10.1007/s002470050661 · Cited by 20

Beckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a child

Sbragia-Neto, L., Filho, A. A. M., Guerra‐Júnior, G., de Lemos‐Marini, S. H. V., Baptista, M. T. M., de Matos, P. S., de Oliveira-Filho, A. G., & Bustorff‐Silva, J. M. (2000) · Journal of Pediatric Surgery · doi:10.1053/jpsu.2000.8771 · Cited by 20

Congenital gastric teratoma in Wiedemann‐Beckwith syndrome

Falik‐Borenstein, T. C., Korenberg, J. R., Davos, I., Platt, L. D., Gans, S. L., Goodman, B. K., Schreck, R. R., & Graham, J. M. (1991) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320380113 · Cited by 20

Cystic Adrenal Masses in the Neonate Associated with Hemihypertrophy and the Relation to the Beckwith-Wiedemann Syndrome

Walton, G. R., Peng, B. C. H., Berdon, W. E., Collins, M. H., & Hensle, T. W. (1991) · The Journal of Urology · doi:10.1016/s0022-5347(17)37861-8 · Cited by 20

Congenital hemihypertrophy and malignant giant pheochromocytoma ? a previously undescribed coincidence

Schnakenburg, K. V., M�ller, M., D�rner, K., Harms, D., Schwarze, E. ‐., Grosse, F. R., & Wiedemann, H. ‐. (1976) · European Journal of Pediatrics · doi:10.1007/bf00481506 · Cited by 19

Regional Proteus syndrome: Report of an autopsy case

Horie, Y., Fujita, H., Mano, S., Kuwajima, M., & Ogawa, K. (1995) · Pathology International · doi:10.1111/j.1440-1827.1995.tb03497.x · Cited by 19

Teratoid Wilms' tumour occurring synchronously with classical Wilms' tumour in Beckwith Wiedemann syndrome

Paterson, A., & Sweeney, L. E. (2000) · Pediatric Radiology · doi:10.1007/s002470000249 · Cited by 19

Beckwith-Wiedemann syndrome and splenic hemangioma: report of a case

Herman, T. E., McAlister, P. W. H., Dehner, L. P., & Skinner, M. (1997) · Pediatric Radiology · doi:10.1007/s002470050149 · Cited by 19

Bilateral calcified ovarian fibromas in a patient with Sotos syndrome

Chen, C., Yang, Y., Lin, S., Wang, W., Chang, C., & Chang, K.-M. (2002) · Fertility and Sterility · doi:10.1016/s0015-0282(02)03118-7 · Cited by 19

Ganglioglioma in a Sotos syndrome patient with an NSD1 deletion

Deardorff, M. A., Maisenbacher, M. K., & Zackai, E. H. (2004) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.30032 · Cited by 19

Screening for cancer in children with Costello syndrome

DeBaun, M. R. (2002) · American Journal of Medical Genetics · doi:10.1002/ajmg.10242 · Cited by 19

Pathology of Osseous and Genitourinary Lesions of Proteus Syndrome

Bale, P. M., Watson, G., & Collins, F. (1993) · Pediatric Pathology · doi:10.3109/15513819309048266 · Cited by 19

Benign Bladder Neck Polyp Causing Tandem Obstruction of the Urinary Tract in a Patient with Beckwith-Wiedemann Syndrome

Bockrath, J. M., Maizels, M., & Firlit, C. F. (1982) · The Journal of Urology · doi:10.1016/s0022-5347(17)53476-x · Cited by 19

Medullary sponge kidneys and unilateral Wilms tumour in a child with Beckwith-Wiedemann syndrome

Beetz, R., Schofer, O., Riedmiller, H. N., Schumacher, R., & Gutjahr, P. (1991) · European Journal of Pediatrics · doi:10.1007/bf01958430 · Cited by 18

Bilateral Wilms's tumour in Klippel-Trenaunay syndrome.

Ehrich, J., Ostertag, H., Flatz, S. D., & Kamran, D. (1979) · Archives of Disease in Childhood · doi:10.1136/adc.54.5.405 · Cited by 17

Nesidioblastosis and Mixed Hamartoma of the Liver in Beckwith-Wiedemann Syndrome: Case Study Including Analysis of H19 Methylation and Insulin-like Growth Factor 2 Genotyping and Imprinting

Fukuzawa, R., Umezawa, A., Morikawa, Y., Kim, K. C., Nagai, T., & Hata, J. (2001) · Pediatric and Developmental Pathology · doi:10.1007/s10024001-0003-8 · Cited by 17

Proteus Syndrome (Report of Three Cases)

Nishimura, G., & Kozlowski, K. S. (1990) · Australasian Radiology · doi:10.1111/j.1440-1673.1990.tb02807.x · Cited by 17

Congenital hemihypertrophy with adrenal carcinoma and medullary sponge kidney

Saypol, D. C., & Laudone, V. E. (1983) · Urology · doi:10.1016/0090-4295(83)90053-5 · Cited by 17

Loss of heterozygosity in non-tumoral tissue in two children with Beckwith-Wiedemann syndrome.

Schneid, H., Vazquez, M., Seurin, D., & Bouc, Y. L. (1991) · PubMed · Cited by 17

Klippel‐Trenauny Syndrome and Cutaneous Carcinomas

Salman, S., Phillips, T. J., & Rogers, G. S. (1993) · The Journal of Dermatologic Surgery and Oncology · doi:10.1111/j.1524-4725.1993.tb00393.x · Cited by 16

Chest wall hamartoma with Wiedemann-Beckwith syndrome: Clinical report and brief review of chromosome 11p15.5-related tumors

Jonas, R. E., & Kimonis, V. E. (2001) · American Journal of Medical Genetics · doi:10.1002/ajmg.1381 · Cited by 16

Angiography and Histopathology of Nephroblastomatosis

Brantley, R. E., & Simson, L. R. (1976) · Radiology · doi:10.1148/120.1.151 · Cited by 16

Cancer in Sotos syndrome

YULE, S. M. (1999) · Archives of Disease in Childhood · doi:10.1136/adc.80.5.493b · Cited by 16

A probable case of familial Weaver syndrome associated with neoplasia

Derry, C. P., TEMPLE, I. K., & VENKAT-RAMAN, K. (1999) · Journal of Medical Genetics · doi:10.1136/jmg.36.9.725 · Cited by 15

Pancreoblastoma in a Neonate Associated with Beckwith-Wiedemann Syndrome

Potts, S. G., Brown, S., & O'Hara, M. A. (1986) · European Journal of Pediatric Surgery · doi:10.1055/s-2008-1043310 · Cited by 15

Proteus Syndrome Associated with a Sacrococcygeal Teratoma; A Rare Combination

Zachariou, Z., Krug, M., Benz, G., & Daum, R. (1996) · European Journal of Pediatric Surgery · doi:10.1055/s-2008-1066522 · Cited by 15

RecurrentNF1 gene mutation in a patient with oligosymptomatic neurofibromatosis type 1 (NF1)

Buske, A., Gewies, A., Lehmann, R., R�ther, K., Algermissen, B., N�rnberg, P., & Tinschert, S. (1999) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19991008)86:4 · Cited by 15

Optic glioma associated with Beckwith-Wiedemann syndrome

Weinstein, J. M., Bačkonja, M., Houston, L., Gilbert, E., Finlay, J. L., Duff, T. A., & Chun, R. W. M. (1986) · Pediatric Neurology · doi:10.1016/0887-8994(86)90026-3 · Cited by 15

Yolk Sac Tumor of the Placenta in Wiedemann-Beckwith Syndrome

Drut, R., Mortera, M., & Drut, R. M. (1998) · Pediatric and Developmental Pathology · doi:10.1007/s100249900073 · Cited by 15

CONGENITAL MESOBLASTIC NEPHROMA IN A CHILD WITH THE BECKWITH-WIEDEMANN SYNDROME

Sutherland, R. W., Wiener, J. S., Hicks, J. M., Hawkins, E. P., & Chintagumpala, M. (1997) · The Journal of Urology · doi:10.1016/s0022-5347(01)64272-1 · Cited by 15

Management Guidelines for Children with Thyroid Nodules and Differentiated Thyroid Cancer

Francis, G. L., Waguespack, S. G., Bauer, A. J., Angelos, P., Benvenga, S., Cerutti, J. M., Dinauer, C., Hamilton, J. K., HAY, I. D., Luster, M., et al. (2015) · Thyroid · doi:10.1089/thy.2014.0460 · Cited by 1,273

Adrenocortical carcinoma

Else, T., Kim, A. C., Sabolch, A., Raymond, V. M., Kandathil, A., Caoili, E. M., Jolly, S., Miller, B. S., Giordano, T. J., & Hammer, G. D. (2014) · Endocrine Reviews · doi:10.1210/er.2013-1029 · Cited by 892

Beckwith–Wiedemann syndrome

Weksberg, R., Shuman, C. T., & Beckwith, J. B. (2009) · European Journal of Human Genetics · doi:10.1038/ejhg.2009.106 · Cited by 690

Hereditary diffuse gastric cancer: updated consensus guidelines for clinical management and directions for future research

Fitzgerald, R. C., Hardwick, R. H., Huntsman, D. D., Carneiro, F., Guilford, P., Blair, V., Chung, D. C., Norton, J. A., Ragunath, K., van Krieken, J. H., et al. (2010) · Journal of Medical Genetics · doi:10.1136/jmg.2009.074237 · Cited by 541

Beckwith–Wiedemann syndrome

Choufani, S., Shuman, C. T., & Weksberg, R. (2010) · American Journal of Medical Genetics Part C Seminars in Medical Genetics · doi:10.1002/ajmg.c.30267 · Cited by 319

Follow-up and Risk of Tumors in Overgrowth Syndromes

Bouthelier, R. G., & Lapunzina, P. D. (2005) · Journal of Pediatric Endocrinology and Metabolism · doi:10.1515/jpem.2005.18.s1.1227 · Cited by 38

Characterization and Childhood Tumor Risk Assessment of Genetic and Epigenetic Syndromes Associated With Lateralized Overgrowth

Griff, J. R., Duffy, K. A., & Kalish, J. M. (2020) · Frontiers in Pediatrics · doi:10.3389/fped.2020.613260 · Cited by 20

Overgrowth syndromes — clinical and molecular aspects and tumour risk

Brioude, F., Toutain, A., Giabicani, É., Cottereau, E., Cormier‐Daire, V., & Netchine, I. (2019) · Nature Reviews Endocrinology · doi:10.1038/s41574-019-0180-z · Cited by 102

Overgrowth syndromes: review of clinical and molecular aspects and tumour risk.

Brioude, F., Toutain, A., Giabicani, É., Cottereau, E., Cormier‐Daire, V., & Netchine, I. (2019) · HAL

Tumour surveillance in Beckwith–Wiedemann syndrome and hemihyperplasia: A critical review of the evidence and suggested guidelines for local practice

Tan, T. Y., & Amor, D. J. (2006) · Journal of Paediatrics and Child Health · doi:10.1111/j.1440-1754.2006.00908.x · Cited by 130