Nonclassical 21-Hydroxylase Deficiency

Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome

(2004) · Fertility and Sterility · doi:10.1016/j.fertnstert.2003.10.004 · Cited by 9,050 · see citing works

Clinical assessment of body hair growth in women.

Ferriman, D., & Gallwey, J. D. (1961) · Journal of Clinical Endocrinology and Metabolism · doi:10.1210/jcem-21-11-1440 · Cited by 2,556 · see citing works

Men at risk: occupation and male infertility.

Claman, P. (2004) · Fertility and Sterility · doi:10.1016/s0015-0282(03)01188-9 · Cited by 2,219 · see citing works

The P450 Superfamily: Update on New Sequences, Gene Mapping, and Recommended Nomenclature

Nebert, D. W., Nelson, D. R., Coon, M. J., Estabrook, R. W., Feyereisen, R., Fujii‐Kuriyama, Y., Gonzalez, F. J., Guengerich, F. P., GUNSALUS, I. C., Johnson, E. F., et al. (1991) · DNA and Cell Biology · doi:10.1089/dna.1991.10.1 · Cited by 1,086 · see citing works

LIPID NEPHROTOXICITY IN CHRONIC PROGRESSIVE GLOMERULAR AND TUBULO-INTERSTITIAL DISEASE

Moorhead, J. F., El-Nahas, M., Chan, M. K., & Varghese, Z. (1982) · The Lancet · doi:10.1016/s0140-6736(82)91513-6 · Cited by 1,070 · see citing works

Classification of the types of androgenetic alopecia (common baldness) occurring in the female sex

Ludwig, E. (1977) · British Journal of Dermatology · doi:10.1111/j.1365-2133.1977.tb15179.x · Cited by 881 · see citing works

Genotyping steroid 21-hydroxylase deficiency: hormonal reference data

NEW, M. I., LORENZEN, F., LERNER, A. J., KOHN, B., OBERFIELD, S. E., POLLACK, M. S., DUPONT, B., STONER, E., LEVY, D. J., PANG, S., et al. (1983) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-57-2-320 · Cited by 624 · see citing works

Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Speiser, P. W., Dupont, J., Zhu, D., Serrat, J., Buegeleisen, M., Tusie-Luna, M. T., Lesser, M., New, M. I., & White, P. C. (1992) · Journal of Clinical Investigation · doi:10.1172/jci115897 · Cited by 572 · see citing works

Structure of human steroid 21-hydroxylase genes.

White, P. C., New, M. I., & Dupont, B. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.14.5111 · Cited by 569 · see citing works

Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene.

Higashi, Y., Yoshioka, H., Yamane, M., Gotoh, O., & Fujii-Kuriyama, Y. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.9.2841 · Cited by 555 · see citing works

High frequency of nonclassical steroid 21-hydroxylase deficiency

SPEISER, P. W., DUPONT, B. O., RUBINSTEIN, P., PIAZZA, A., KASTELAN, A., & NEW, M. I. (1986) · Obstetrical & Gynecological Survey · doi:10.1097/00006254-198604000-00017 · Cited by 523 · see citing works

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man

White, P. C., Grossberger, D., Onufer, B. J., Chaplin, D. D., New, M. I., Dupont, B., & Strominger, J. L. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.4.1089 · Cited by 490 · see citing works

The structural basis of the multiple forms of human complement component C4

Belt, K., Carroll, M. C., & Porter, R. R. (1984) · Cell · doi:10.1016/0092-8674(84)90040-0 · Cited by 417 · see citing works

Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency)

Dupont, B., Oberfield, S. E., Smithwick, E. M., Lee, T. D., & Levine, L. S. (1977) · The Lancet · doi:10.1016/s0140-6736(77)90362-2 · Cited by 371 · see citing works

Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.

Carroll, M. C., Campbell, R. D., & Porter, R. R. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.2.521 · Cited by 370 · see citing works

Steroid 21-hydroxylase deficiency: genotype may not predict phenotype

Wilson, R. C. (1995) · Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.80.8.2322 · Cited by 324 · see citing works

HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.

White, P. C., New, M. I., & Dupont, B. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.23.7505 · Cited by 292 · see citing works

The human gene mutation database

Krawczak, M. (1997) · Trends in Genetics · doi:10.1016/s0168-9525(97)01068-8 · Cited by 261 · see citing works

Determination of functional effects of mutations in the steroid 21-hydroxylase gene (CYP21) using recombinant vaccinia virus.

Tusie-Luna, M. T., Traktman, P., & White, P. C. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)45304-x · Cited by 254 · see citing works

Mutation in the CYP21B gene (Ile-172-Asn) causes steroid 21-hydroxylase deficiency

Amor, M., Parker, K. L., Globerman, H., New, M. I., & White, P. C. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.5.1600 · Cited by 251 · see citing works

Aberrant splicing and missense mutations cause steroid 21-hydroxylase [P-450(C21)] deficiency in humans: possible gene conversion products

Higashi, Y., Tanae, A., Inoue, H., Hiromasa, T., & Fujii-Kuriyama, Y. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.20.7486 · Cited by 244 · see citing works

Gender development in women with congenital adrenal hyperplasia as a function of disorder severity

Meyer-Bahlburg, H. F. L., Dolezal, C., Baker, S. W., Ehrhardt, A. A., & New, M. I. (2006) · Archives of Sexual Behavior · doi:10.1007/s10508-006-9068-9 · Cited by 234 · see citing works

Molecular Genetic Analysis of Nonclassic Steroid 21-Hydroxylase Deficiency Associated with HLA-B14,DR1

Speiser, P. W., New, M. I., & White, P. C. (1988) · New England Journal of Medicine · doi:10.1056/nejm198807073190104 · Cited by 205 · see citing works

Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia

KOHN, B., LEVINE, L. S., POLLACK, M. S., PANG, S., LORENZEN, F., LEVY, D., LERNER, A. J., RONDANINI, G. F., DUPONT, B., & NEW, M. I. (1982) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-55-5-817 · Cited by 204 · see citing works

Long Term Outcome in Adult Males with Classic Congenital Adrenal Hyperplasia1

Cabrera, M. S., Vogiatzi, M. G., & New, M. I. (2001) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.86.7.7668 · Cited by 204 · see citing works

Effects of Individual Mutations in the P-450(C21) Pseudogene on the P-450(C21) Activity and Their Distribution in the Patient Genomes of Congenital Steroid 21-Hydroxylase Deficiency1

Higashi, Y., Hiromasa, T., Tanae, A., Miki, T., Nakura, J., Kondo, T., Ohura, T., Ogawa, E., Nakayama, K., & Fujii-Kuriyama, Y. (1991) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a123433 · Cited by 201 · see citing works

Adult Height and Fertility in Men with Congenital Virilizing Adrenal Hyperplasia

Urban, M. D., Lee, P. A., & Migeon, C. J. (1978) · New England Journal of Medicine · doi:10.1056/nejm197812212992505 · Cited by 198 · see citing works

Androgen Excess in Cystic Acne

Marynick, S. P., Chakmakjian, Z. H., McCaffree, D. L., & Herndon, J. H. (1983) · New England Journal of Medicine · doi:10.1056/nejm198304283081701 · Cited by 193 · see citing works

A Mutation (Pro-30 to Leu) in<i>CYP</i>21 Represents a Potential Nonclassic Steroid 21-Hydroxylase Deficiency Allele

Tusie-Luna, M.-T., Speiser, P. W., Dumic, M., New, M. I., & White, P. C. (1991) · Molecular Endocrinology · doi:10.1210/mend-5-5-685 · Cited by 183 · see citing works

Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excess

New, M. I., & Wilson, R. C. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.22.12790 · Cited by 164 · see citing works

Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency.

(1991) · Europe PMC (PubMed Central) · Cited by 164 · see citing works

Adult manifestation of congenital adrenal hyperplasia due to incomplete 21-hydroxylase deficiency mimicking polycystic ovarian disease

Løbo, R. A., & Goebelsmann, U. (1980) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(80)90095-2 · Cited by 157 · see citing works

Adrenal Androgen Hyperresponsiveness to Adrenocorticotropin in Women with Acne and/or Hirsutism: Adrenal Enzyme Defects and Exaggerated Adrenarche*

Lucky, A. W., Rosenfield, R. L., McGUIRE, J., Rudy, S. J., & Helke, J. (1986) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-62-5-840 · Cited by 156 · see citing works

Clinical and Biological Phenotypes in Late-Onset 21 Hydroxylase Deficiency

DEWAILLY, D., VANTYGHEM-HAUDIQUET, M.-C., SAINSARD, C., BUVAT, J., CAPPOEN, J. P., ARDAENS, K., RACADOT, A., LEFEBVRE, J., & FOSSATI, P. (1986) · The Journal of Clinical Endocrinology &amp; Metabolism · doi:10.1210/jcem-63-2-418 · Cited by 151 · see citing works

Genetic Defects of Steroidogenesis in Premature Pubarche*

Temeck, J. W., Pang, S., Nelson, C. P., & New, M. I. (1987) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-64-3-609 · Cited by 150 · see citing works

A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency.

Chiou, S. H., Hu, M. C., & Chung, B. C. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)39804-7 · Cited by 149 · see citing works

Growth of Patients with 21-Hydroxylase Deficiency: An Analysis of the Factors Influencing Adult Height

Jääskeläinen, J., & Voutilainen, R. (1997) · Pediatric Research · doi:10.1203/00006450-199701000-00005 · Cited by 144 · see citing works

Phenotype-Genotype Correlation in 56 Women with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Deneux, C., Tardy, V., Dib, A., Mornet, E., Billaud, L., Charron, D., Morel, Y., & Kuttenn, F. (2001) · The Journal of Clinical Endocrinology &amp; Metabolism · doi:10.1210/jc.86.1.207 · Cited by 144 · see citing works

Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene

Wilson, R. C., Wei, J., Cheng, K. C., Mercado, A. B., & New, M. I. (1995) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.80.5.7745011 · Cited by 134 · see citing works

Two steroid 21-hydroxylase genes are located in the murine S region

White, P. C., Chaplin, D., Weis, J. H., Dupont, B., New, M. I., & Seidman, J. G. (1984) · Nature · doi:10.1038/312465a0 · Cited by 133 · see citing works

Nonsense mutation causing steroid 21-hydroxylase deficiency

Globerman, H., Amor, M., Parker, K. L., New, M. I., & White, P. C. (1988) · Journal of Clinical Investigation · doi:10.1172/jci113562 · Cited by 130 · see citing works

Frequent deletion and duplication of the steroid 21-hydroxylase genes.

WERKMEISTER, J. W., New, M. I., Dupont, B., & White, P. C. (1986) · PubMed · Cited by 129 · see citing works

Mutations in steroid 21-hydroxylase (CYP21)

White, P. C., Tusie-Luna, M.-T., New, M. I., & Speiser, P. W. (1994) · Human Mutation · doi:10.1002/humu.1380030408 · Cited by 129 · see citing works

R339H and P453S: CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversions.

Helmberg, A., Tusie-Luna, M. T., Tabarelli, M., Kofler, R., & White, P. C. (1992) · Molecular Endocrinology · doi:10.1210/mend.6.8.1406709 · Cited by 123 · see citing works

Treatment with growth hormone and luteinizing hormone releasing hormone analog improves final adult height in children with congenital adrenal hyperplasia

Lin-Su, K., Vogiatzi, M. G., Marshall, I., Harbison, M. D., Macapagal, M. C., Betensky, B., Tansil, S., & New, M. I. (2005) · The Journal of Clinical Endocrinology &amp; Metabolism · doi:10.1210/jc.2004-2128 · Cited by 111 · see citing works

Cryptic 21-Hydroxylase Deficiency in Families of Patients with Classical Congenital Adrenal Hyperplasia*

Levine, L. S., Dupont, B., LORENZEN, F., PANG, S., Pollack, M. S., Oberfield, S. E., Kohn, B., Lerner, A. J., CACCIARI, E., Mantero, F., et al. (1980) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-51-6-1316 · Cited by 111 · see citing works

Untitled work

(1988) · PubMed · Cited by 110 · see citing works

Cloning and expression of cDNA encoding a bovine adrenal cytochrome P-450 specific for steroid 21-hydroxylation.

White, P. C., New, M. I., & Dupont, B. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.7.1986 · Cited by 107 · see citing works

An Attenuated Form of Congenital Virilizing Adrenal Hyperplasia*

Rosenwaks, Z., Lee, P. A., Jones, G. S., Migeon, C. J., & Wentz, A. C. (1979) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-49-3-335 · Cited by 102 · see citing works

CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency

Balsamo, A., Cicognani, A., Baldazzi, L., Barbaro, M., Baronio, F., Gennari, M., Bal, M., Cassio, A., Kontaxaki, K., & Cacciari, E. (2003) · The Journal of Clinical Endocrinology &amp; Metabolism · doi:10.1210/jc.2003-030123 · Cited by 102 · see citing works

Follow-Up of 68 Children with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Relevance of Genotype for Management

Pinto, G., Tardy, V., Trivin, C., Thalassinos, C., Lortat-Jacob, S., Nihoul-Fékété, C., Morel, Y., & Brauner, R. (2003) · The Journal of Clinical Endocrinology &amp; Metabolism · doi:10.1210/jc.2002-021433 · Cited by 101 · see citing works

Fertility in Women With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Stikkelbroeck, N. M. M. L., Hermus, A. R., Braat, D. D. M., & Otten, B. J. (2003) · Obstetrical & Gynecological Survey · doi:10.1097/01.ogx.0000062966.93819.5b · Cited by 95 · see citing works

High Incidence of Molecular Defects of the CYP21 Gene in Patients with Premature Adrenarche

Dacou‐Voutetakis, C., & Dracopoulou, M. (1999) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.84.5.5683 · Cited by 95 · see citing works

Male infertility due to congenital adrenal hyperplasia: testicular biopsy findings, hormonal evaluation, and therapeutic results in three patients

Bonaccorsi, A. C., Adler, I., & Figueiredo, J. G. (1987) · Fertility and Sterility · doi:10.1016/s0015-0282(16)59119-5 · Cited by 93 · see citing works

A multicenter study of women with nonclassical congenital adrenal hyperplasia: relationship between genotype and phenotype

Speiser, P. W., Knochenhauer, E. S., Dewailly, D., Fruzzetti, F., Marcondes, J. A. M., & Azziz, R. (2000) · Molecular Genetics and Metabolism · doi:10.1006/mgme.2000.3036 · Cited by 89 · see citing works

Steroid 21-hydroxylase (P450c21): a new allele and spread of mutations through the pseudogene

Wedell, A., & Luthman, H. (1993) · Human Genetics · doi:10.1007/bf00218263 · Cited by 81 · see citing works

Rearrangement of 21-hydroxylase genes in disease-associated MHC supratypes

Garlepp, M. J., Wilton, A. N., Dawkins, R. L., & White, P. C. (1986) · Immunogenetics · doi:10.1007/bf00377968 · Cited by 80 · see citing works

The effect of treatment of final height in classical congenital adrenal hyperplasia (CAH)

DiMartino-Nardi, J., Stoner, E., O'Connell, A., & New, M. I. (1986) · European Journal of Endocrinology · doi:10.1530/acta.0.112s305 · Cited by 79 · see citing works

Abnormal Adrenal Responses to Adrenocorticotropic Hormone in Hyperandrogenic Women

Gibson, M., Lackritz, R. M., Schiff, I., & Tulchinsky, D. (1980) · Fertility and Sterility · doi:10.1016/s0015-0282(16)44475-4 · Cited by 77 · see citing works

Isolated precocious pubarche: an approach

Balducci, R., Boscherini, B., Mangiantini, A., Morellini, M., & Toscano, V. (1994) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.79.2.8045980 · Cited by 72 · see citing works

“ACQUIRED” ADRENAL HYPERPLASIA WITH 21-HYDROXYLASE DEFICIENCY IS NOT THE SAME GENETIC DISORDER AS CONGENITAL ADRENAL HYPERPLASIA

New, M. I., LORENZEN, F., PANG, S., Günczler, P., Dupont, B., & Levine, L. S. (1979) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-48-2-356 · Cited by 71 · see citing works

Prevalence of ovarian adrenal rest tumours and polycystic ovaries in females with congenital adrenal hyperplasia: results of ultrasonography and MR imaging

Stikkelbroeck, N. M. L., Hermus, A. M. M., Schouten, D., Suliman, H., Jager, G., Braat, D. M., & Otten, B. (2004) · European Radiology · doi:10.1007/s00330-004-2329-x · Cited by 71 · see citing works

Carrier status for steroid 21-hydroxylase deficiency is only one factor in the variable phenotype of acne

Ostlere, L. S., Rumsby, G., Holownia, P., Jacobs, H. S., Rustin, M. H. A., & Honour, J. W. (1998) · Clinical Endocrinology · doi:10.1046/j.1365-2265.1998.00381.x · Cited by 70 · see citing works

Long Term Outcome in Adult Males With Classic Congenital Adrenal Hyperplasia

Jarow, J. P. (2002) · The Journal of Urology · doi:10.1097/00005392-200208000-00120 · Cited by 66 · see citing works

REVERSIBLE MALE INFERTILITY DUE TO CONGENITAL ADRENAL HYPERPLASIA

WISCHUSEN, J., Baker, H. W. G., & Hudson, B. (1981) · Clinical Endocrinology · doi:10.1111/j.1365-2265.1981.tb02967.x · Cited by 64 · see citing works

Prevalence of Nonclassical Steroid 21-Hydroxylase Deficiency Based on a Morning Salivary 17-hydroxyprogesterone Screening Test: A Small Sample Study*

Zerah, M., Ueshiba, H., Wood, E. A., Speiser, P., Crawford, C., MCDONALD, T., PAREIRA, J., Gruen, D., & New, M. I. (1990) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-70-6-1662 · Cited by 59 · see citing works

Genotype‐phenotype analysis in late onset 21‐hydroxylase deficiency in comparison to the classical forms

Rumsby, Avey, Conway, & Honour (1998) · Clinical Endocrinology · doi:10.1046/j.1365-2265.1998.00402.x · Cited by 59 · see citing works

Untitled work

(1988) · PubMed · Cited by 59 · see citing works

The Effect of Long Acting Glucocorticoids on Menstrual Abnormalities in Patients with Virilizing Congenital Adrenal Hyperplasia*

Richards, G. E., Grumbach, M. M., Kaplan, S. L., & Conte, F. A. (1978) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-47-6-1208 · Cited by 56 · see citing works

Ovarian `Tumor' of the Adrenogenital Syndrome

Al‐Ahmadie, H. A., Stanek, J. W., LIU, J. H., Mangu, P. N., Niemann, T., & Young, R. H. (2001) · The American Journal of Surgical Pathology · doi:10.1097/00000478-200111000-00015 · Cited by 55 · see citing works

Growth and body proportions in congenital adrenal hyperplasia.

Young, M. C., Ribeiro, J., & Hughes, I. A. (1989) · Archives of Disease in Childhood · doi:10.1136/adc.64.11.1554 · Cited by 55 · see citing works

Early growth is not increased in untreated moderately severe 21‐hydroxylase deficiency

Thilén, A., Woods, K., Perry, L., Savage, M. O., Wedell, A., & Ritzén, E. M. (1995) · Acta Paediatrica · doi:10.1111/j.1651-2227.1995.tb13788.x · Cited by 53 · see citing works

Validation and Clinical Application of a Locus-Specific Polymerase Chain Reaction- and Minisequencing-Based Assay for Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency)

Keen‐Kim, D., Redman, J. B., Alanes, R. U., Eachus, M. M., Wilson, R. C., New, M. I., Nakamoto, J. M., & Fenwick, R. G. (2005) · Journal of Molecular Diagnostics · doi:10.1016/s1525-1578(10)60550-8 · Cited by 52 · see citing works

Functional Analysis of Two Recurrent Amino Acid Substitutions in theCYP21Gene from Italian Patients with Congenital Adrenal Hyperplasia

Barbaro, M., Lajić, S., Baldazzi, L., Balsamo, A., Pirazzoli, P., Cicognani, A., Wedell, A., & CACCIARI, E. (2004) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2003-031630 · Cited by 51 · see citing works

Ovarian adrenal-like tissue in congenital adrenal hyperplasia

Russo, G., Paesano, P., Taccagni, G., Del Maschio, A., & Chiumello, G. (1998) · New England Journal of Medicine · doi:10.1056/nejm199809173391220 · Cited by 50 · see citing works

Reversible male infertility in late onset congenital adrenal hyperplasia

Augarten, A., Weissenberg, R., Pariente, C., & Sack, J. (1991) · Journal of Endocrinological Investigation · doi:10.1007/bf03346799 · Cited by 47 · see citing works

Adrenal Steroidogenic Function in a Black and Hispanic Population with Precocious Pubarche

Oberfield, S. E., Mayes, D. M., & Levine, L. S. (1990) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-70-1-76 · Cited by 44 · see citing works

Phenotype and genotype correlation of the microconversion from the CYP21A1P to the CYP21A2 gene in congenital adrenal hyperplasia

Torres, N., de Mello, M. P., Germano, C. M. R., Elias, L. L. K., Moreira, A. C., & de Castro, M. (2003) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x2003001000006 · Cited by 43 · see citing works

ADRENAL STEROIDOGENESIS IN HIRSUTE WOMEN

Child, D. F., Bu'Lock, D. E., & Anderson, D. C. (1980) · Clinical Endocrinology · doi:10.1111/j.1365-2265.1980.tb01381.x · Cited by 42 · see citing works

A Novel Semiquantitative Polymerase Chain Reaction/Enzyme Digestion-Based Method for Detection of Large Scale Deletions/Conversions of the CYP21 Gene and Mutation Screening in Turkish Families with 21-Hydroxylase Deficiency

Tükel, T., Uyguner, Z. O., Wei, J., Yüksel‐Apak, M., Saka, N., Song, D.-X., Kayserili, H., Baş, F., Günöz, H., Wilson, R. C., et al. (2003) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2003-030813 · Cited by 42 · see citing works

Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Speisere, P. W., New, M. I., Tannin, G. M., Pickering, D. E., Yang, S. Y., & White, P. C. (1992) · Human Genetics · doi:10.1007/bf02265290 · Cited by 42 · see citing works

17-Hydroxyprogesterone Responses to Adrenocorticotropin in Children with Premature Adrenarche*

Granoff, A. B., Chasalow, F. I., & Blethen, S. L. (1985) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-60-3-409 · Cited by 42 · see citing works

Unilateral Testicular Enlargement Resulting from Inapparent 21-Hybroxylase Deficiency

Chrousos, G. P., Loriaux, D. L., Sherins, R. J., & Cutler, G. B. (1981) · The Journal of Urology · doi:10.1016/s0022-5347(17)54411-0 · Cited by 36 · see citing works

Frequent Deletion and Duplication of the Steroid 21-Hydroxylase Genes

WERKMEISTER, J. W., New, M. I., Dupont, B., & White, P. C. (1987) · Obstetrical & Gynecological Survey · doi:10.1097/00006254-198709000-00015 · Cited by 34 · see citing works

An update on the frequency of nonclassic deficiency of adrenal 21-hydroxylase in the Yugoslav population

Dumić, M., Brkljačić, L., Speiser, P. W., Wood, E., Crawford, C., Plavšić, V., Baničeviác, M., Radmanović, S., Radica, A., Kaštelan, A., et al. (1990) · Acta Endocrinologica · doi:10.1530/acta.0.1220703 · Cited by 33 · see citing works

[Final height in 69 patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency].

David, M., Sempe, M., Blanc, M., Nicolino, M. P., Forest, M., & Morel, Y. (1994) · PubMed · Cited by 32 · see citing works

The Partial Adrenocortical Hydroxylase Deficiency Syndrome in Infertile Women

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Update: Prenatal Diagnosis for Congenital Adrenal Hyperplasia in 595 Pregnancies

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