Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report

Consanguinity, human evolution, and complex diseases

Bittles, A. H., & Black, M. L. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906079106 · Cited by 646

Consanguinity and reproductive health among Arabs

Tadmouri, G. O., Nair, P., Obeid, T., Ali, M. T. A., Khaja, N. A., & Hamamy, H. (2009) · Reproductive Health · doi:10.1186/1742-4755-6-17 · Cited by 642

Consanguinity and its relevance to clinical genetics

Bittles, A. H. (2001) · Clinical Genetics · doi:10.1034/j.1399-0004.2001.600201.x · Cited by 602

Reproductive Behavior and Health in Consanguineous Marriages

Bittles, A. H., Mason, W. M., Greene, J., & Rao, N. A. (1991) · Science · doi:10.1126/science.2028254 · Cited by 331

Mutations in PYCR1 cause cutis laxa with progeroid features

Reversade, B., Escande‐Beillard, N., Dimopoulou, A., Fischer‐Zirnsak, B., Chng, S. C., Li, Y., Shboul, M., Tham, P.-Y., Kayserili, H., Al‐Gazali, L., et al. (2009) · Nature Genetics · doi:10.1038/ng.413 · Cited by 262

Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors

Bennett, R. L., Motulsky, A. G., Bittles, A. H., Hudgins, L., Uhrich, S. B., Doyle, D. L., Silvey, K., Scott, C. R., Cheng, E., McGillivray, B., et al. (2002) · Journal of Genetic Counseling · doi:10.1023/a:1014593404915 · Cited by 234

Consanguineous marriage in Jordan

Khoury, S., & Massad, D. (1992) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320430502 · Cited by 219

Genetic Disorders Among Arab Populations

Teebi, A. S. (2010) · Springer eBooks · doi:10.1007/978-3-642-05080-0 · Cited by 162

CONSANGUINEOUS MARRIAGE IN A NEWLY DEVELOPED COUNTRY: THE QATARI POPULATION

Bener, A., & Alali, K. (2004) · Journal of Biosocial Science · doi:10.1017/s0021932004007060 · Cited by 160

Contribution of BRCA1 and BRCA2 Mutations to Breast and Ovarian Cancer in Pakistan

Liede, A., Malik, I. A., Aziz, Z., Rios, P. D. L., Kwan, E., & Narod, S. A. (2002) · The American Journal of Human Genetics · doi:10.1086/342506 · Cited by 159

Consanguineous marriage as a key indicator of isolated congenital dental anomaly among South Indian population – A cross-sectional study

Rajeswari, M. R. C., Ramamoorthy, A., Rajakumar, A. S., & Narayan, V. K. (2023) · Journal of Oral and Maxillofacial Pathology · doi:10.4103/jomfp.jomfp_265_21 · Cited by 4

Exploring perceptions of consanguineous unions with women from an East London community: analysis of discussion groups

Cupp, M. A., Adams, M., Heys, M., Lakhanpaul, M., Alexander, E. C., Milner, Y., Huq, T., Peachey, M., Shah, L., Mirza, I. S., et al. (2019) · Journal of Community Genetics · doi:10.1007/s12687-019-00429-4 · Cited by 4

c.1227_1228dupGG (p.Glu410Glyfs), a frequent variant in Tunisian patients with MUTYH associated polyposis

Kdissa, A., Brusgaard, K., Ksiaa, M., Golli, L., Hallara, O., Ousager, L. B., Manoubi, W., Sghaier, R. B., Adala, L., Halleb, Y., et al. (2019) · Cancer Genetics · doi:10.1016/j.cancergen.2019.10.007 · Cited by 4

A Protocol for Preconceptional Screening of Consanguineous Couples Using Whole Exome Sequencing

dos Santos, C. M. D. A., Heller, A. H., Pena, H. B., & Pena, S. D. J. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.685123 · Cited by 4

Les mariages consanguins et leurs effets sur les maladies non transmissibles dans la population Marocaine: étude transversale

Goundali, K. E., Bouab, C., Rifqi, L., Chebabe, M., & Hilali, A. (2022) · Pan African Medical Journal · doi:10.11604/pamj.2022.41.221.31273 · Cited by 4

Consanguinity, Fertility and Reproductive Outcomes: An International Review

Jaber, L., Nashif, A., & Diamond, G. W. (2023) · Medical Research Archives · doi:10.18103/mra.v11i7.1.4051 · Cited by 4

Congenital Cataracts; Its Laterality and Association with Consanguinity

Rana, A. M., Raza, A. S., Akhter, W., & Rana, M. (2014) · Pakistan Journal of Ophthalmology · doi:10.36351/pjo.v30i4.198 · Cited by 4

Association of Xmn1 polymorphism and consanguineous marriage with fetal hemoglobin in Syrian patients with sickle cell disease

Kahhaleh, F. G., Sulaiman, M. A., & Al-Quobaili, F. (2019) · Cogent Medicine · doi:10.1080/2331205x.2019.1639243 · Cited by 4

The Abundance of Harmful Rare Homozygous Variants in Children of Consanguineous Parents

Subramanian, S. (2025) · Biology · doi:10.3390/biology14030310 · Cited by 3

Exploring the unique characteristics of genes with dual autosomal dominant and recessive inheritance: mechanisms, phenotypes and candidate identification

Ezer, S., Sido, T., Rips, J., Hoffman-Lipschuetz, R., Fuchs, A., Abu‐Libdeh, B., Chervinsky, E., Damseh, N. S., Danial‐Farran, N., Morani, I., et al. (2025) · Journal of Medical Genetics · doi:10.1136/jmg-2025-110872 · Cited by 3

Identification of a Novel GRM1 Frameshift Variant in Two Pakistani Families Broadens the Genetic Landscape of Ultra-Rare Spinocerebellar Ataxia Type 13

Ahmad, R., Zamani, M., Self, E., Shah, S. U. D., Naeem, M. S., & Houlden, H. (2025) · The Cerebellum · doi:10.1007/s12311-025-01897-w · Cited by 3

Consanguineous Marriage in Global Perspective: Anthropological Roots, Genetic Risks, Contemporary Relevance, and the Way Forward

Kalam, M. A., & Pal, S. (2025) · Nature anthropology · doi:10.70322/natanthropol.2025.10023 · Cited by 3

Consanguinity in the Lebanese population: knowledge, attitudes and practices

Chouery, É., Ibrahim, J.-N., Deeb, M. E., Sobh, A., Ghanem, M., Sobh, J., Choueiry, F. E., Rashwan, R., Swaidan, D., Abdelrazzak, A., et al. (2026) · Journal of Community Genetics · doi:10.1007/s12687-026-00874-y · Cited by 3

Going Back to Fundamentals: Three Marriageable Actions for Thalassemia and Carrier Population Management

Kim, S., Dhaheri, H. A., & Kim, S.-Y. (2022) · Thalassemia Reports · doi:10.3390/thalassrep12030016 · Cited by 3

Consanguineous Marriages and Child Ever Born—The Moderating Role of Working Women

Saleem, M. U., Khatir, A. G., Shah, A. A., & Jiang, Q. (2025) · American Journal of Human Biology · doi:10.1002/ajhb.70043 · Cited by 3

Community genetic services in Arab countries

Hamamy, H. (2012) · Middle East Journal of Medical Genetics · doi:10.1097/01.mxe.0000422777.67364.e5 · Cited by 3

Applied cultural and social studies are needed for a sustainable reduction of genetic disease incidence

Staal, J. (2017) · European Journal of Sociology and Anthropology · doi:10.20897/ejsa.201701 · Cited by 3

Characteristics of patients attending the child and adolescent psychiatric outpatient clinic in Erbil city

Abdulqader, S. A., & Saeed, B. A. (2019) · PLoS ONE · doi:10.1371/journal.pone.0209418 · Cited by 4

Twin births in Jordan: incidence, trends, risk factors and implications for under-five mortality: evidence from the 2012 Jordan Population and Family Health Survey

Islam, M. M., & Marium, U. (2019) · Journal of Biosocial Science · doi:10.1017/s0021932019000154 · Cited by 3

Consanguineous Marriage and the Psychopathology of the Progeny of First-Cousin Couples

Shaw, A. (2018) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2018.0513 · Cited by 3

Autistic behavior is a common outcome of biallelic disruption of PDZD8 in humans and mice

Pantiru, A., de Sompele, S. V., Ligneul, C., Chatelain, C., Barrea, C., Lerch, J. P., Filippi, B., Alkan, S., Baere, E. B. W. D., Johnston, J., et al. (2025) · Molecular Autism · doi:10.1186/s13229-025-00650-8 · Cited by 4

Prevalence of Congenital Anomalies and Predictive Factors in Pregnant Women in Bahrain: A Retrospective Analysis

Buhasan, A., Zayer, L. A., Al-Jabery, L., Mohamed, A., Madhoob, A. A., Zaman, E., & Jeddy, R. (2025) · Life · doi:10.3390/life15040650 · Cited by 2

Claiming normal: Disability, stigma, and relationality in Amman

Sargent, C. (2025) · Medical Anthropology Quarterly · doi:10.1111/maq.70003 · Cited by 1

Consanguinity between Parents and Risk of Epilepsy among Children in Northern Saudi Arabia

Alanazi, Y. W., & Jabrah, M. A. A. A. A. (2018) · The Egyptian Journal of Hospital Medicine · doi:10.21608/ejhm.2018.9393 · Cited by 2

Detection of Risk Factor Interactions in Cerebral Palsy Using Statistical Methods

Bakhshi, E., Delavar, S. Z., Soleimani, F., & Biglarian, A. (2018) · Iranian Journal of Pediatrics · doi:10.5812/ijp.57202 · Cited by 2

Molecular Genetic Testing in Pediatric and Adult Neurology in Iraq: New Experience and Challenges from a Developing Country

Saadi, N. W., Yassin, B. A. G., Makhseed, N., & Hadi, A. S. (2020) · Journal of Pediatric Neurology · doi:10.1055/s-0040-1716365 · Cited by 2

Assessment of Awareness on the Risk of Consanguineous Marriages among University Students from Four Developing Countries: A Comparative Study

Ibrahim, Z., & Serakıncı, N. (2020) · HAL · Cited by 2

Genetic analysis based on 15 autosomal short tandem repeats (STRs) in the Chaouia population, western center Morocco, and genetic relationships with worldwide populations

Cheffi, K., Khair, A. E., Dahbi, N., Talbi, J., Hilali, A., & Ossmani, H. E. (2023) · Molecular Genetics and Genomics · doi:10.1007/s00438-023-02028-y · Cited by 2

Uptake rate of carrier screening among consanguineous couples

Ricca, J., Brandt, J. S., Jacob, N., & Ashkinadze, E. (2024) · Prenatal Diagnosis · doi:10.1002/pd.6556 · Cited by 2

Analyzing Cardiovascular Disease Research in the Arab Region: A Bibliometric Review From 2012 to 2022

Hani, A. B., Tarazi, A., Hamadneh, Y. I., Al-Samahan, A., Awad, R., Kan’an, M., Al-Kasaji, M., & Younes, N. A. (2024) · International Journal of Vascular Medicine · doi:10.1155/2024/5915132 · Cited by 2

Consanguinity in twenty-first century India

Kalam, M. A., & Pal, S. (2024) · Journal of bioanthropology · doi:10.54062/jb.4.3.2 · Cited by 2

A genomic tale of inbreeding in western Mediterranean human populations

Hernández, C. L., Sánchez-Martínez, L. J., Ceballos, F. C., Dugoujon, J. M., Pereira, L., & Calderón, R. (2025) · Human Genetics · doi:10.1007/s00439-025-02747-9 · Cited by 2

Prevalence and clinical characteristics of Keratoconus amongst school children in Mumbai

Chaurasia, N., Moodley, V. R., & Mashige, K. P. (2025) · Contact Lens and Anterior Eye · doi:10.1016/j.clae.2025.102444 · Cited by 2

Next Generation Sequencing as an Emerging Technology in Rare Disease Genetics

Rasheed, M. (2020) · Journal of Islamabad Medical & Dental College · doi:10.35787/jimdc.v9i1.521 · Cited by 2

Association of Parental Consanguinity With Papillary Thyroid Carcinoma: A Case-Control Study

Zayed, A. A., Amarin, J. Z., Al-Ani, A. T., Altell, T., Abdelhamid, S. S., Qirem, M., Fahmawi, S. M., Elshebli, S., Hamo, K. M., Zaghlol, L. Y., et al. (2021) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgab071 · Cited by 2

Effect of Women’s Status on Consanguinity in the Arab Society of Israel

Zalan, A. A., Khatib, M., Muhammad, A. S., Mahajnah, M. M., Atamany, E., & Sharkia, R. A. (2022) · Advances in Anthropology · doi:10.4236/aa.2022.123011 · Cited by 2

Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome

Kelmemi, W., Teeuw, M. E., Bochdanovits, Z., Ouburg, S., Jonker, M. A., Alkuraya, F. S., Hashem, M., Kayserili, H., van Haeringen, A., Sheridan, E. G., et al. (2015) · BMC Medical Genetics · doi:10.1186/s12881-015-0191-0 · Cited by 2

The Implications of Parental Consanguinity on the Care of Neonates

Ng, D. S. (2016) · Advances in Neonatal Care · doi:10.1097/anc.0000000000000317 · Cited by 2

CLCC1 c. 75C>A Mutation in Pakistani Derived Retinitis Pigmentosa Families Likely Originated With a Single Founder Mutation 2,000–5,000 Years Ago

Ma, Y., Wang, X., Shoshany, N., Jiao, X., Lee, A. C., Ku, G., Baple, E. L., Fasham, J., Nadeem, R., Naeem, M. A., et al. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.804924 · Cited by 2

Impact of consanguinity on spontaneous pregnancy loss and descendants’ health in north Morocco

Hardouz, H., Arfaoui, A., & Quyou, A. (2023) · Arab Gulf Journal of Scientific Research · doi:10.1108/agjsr-01-2023-0027 · Cited by 2

Association of Different Type of Refractive Errors with Parental Cousin Marriages

Awais, A., Akram, S., Awais, D., Arshad, A., & Hassan, Z. (2023) · Pakistan Journal of Health Sciences · doi:10.54393/pjhs.v4i05.537 · Cited by 2

Practice of Consanguinity and Unusual Cases of Inherited Familial Chromosome Abnormalities: A Case Report.

Sanyal, D., Bhairi, V., & Kadandale, J. S. (2016) · Europe PMC (PubMed Central) · Cited by 2

Founder Variants of the Turkish.

Kablan, A. (2026) · Clinical genetics · doi:10.1111/cge.70080 · Cited by 1

Discovery of a novel cystathionine-beta-synthase mutation and diagnosis of homocystinuria by whole exome sequencing in a family from rural Honduras

Turner, S. A., Dinulos, M. B., Vallee, S. E., Kennedy, L. S., Mason, P., Seibert, D. J., Martinez, M. T., Steinmetz, H. B., Tsongalis, G. J., & Lefferts, J. A. (2015) · Case Reports in Clinical Pathology · doi:10.5430/crcp.v2n3p59 · Cited by 1

Consanguinité, Isonymie et Age Précoce au Mariage dans les deux Provinces de Tétouan et M’diq-fnideq (Maroc)

Hajjaji, M., Khadmaoui, A., Soulaymani, A., & Azzouzi, Y. (2018) · European Scientific Journal ESJ · doi:10.19044/esj.2018.v14n25p63 · Cited by 1

Improved efficiency and patient safety through bespoke electronic thalassaemia care module

Naveed, M., AlSerkal, Y. M., Al-Nuaimi, S., Al-Blooshi, K., Al-Mahiri, N. M., Khan, Y. M. A., Naqvi, S. A., & Preman, N. (2019) · BMJ Health & Care Informatics · doi:10.1136/bmjhci-2019-100094 · Cited by 1

People’s Perception about Consanguineous Marriages and Child Health Issues: A Case Study in Gujranwala

Rizwana, M. (2020) · Pakistan Social Sciences Review · doi:10.35484/pssr.2020(4-iv)15 · Cited by 1

Recessive diseases and founder genetics

Puffenberger, E. G. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820140-4.00012-0 · Cited by 1

INCIDENCE OF CONSANGUINITY IN INDIAN CHILDREN WITH CEREBRAL PALSY: A SURVEY STUDY

Rashmi, H. A., Shailaja, U., & Rao, P. N. (2021) · International Journal of Research in Ayurveda and Pharmacy · doi:10.7897/2277-4343.120370 · Cited by 1

Live Birth of a Healthy Child in a Couple with Identical mtDNA Carrying a Pathogenic c.471_477delTTTAAAAinsG Variant in the MOCS2 Gene

Tofilo, M., Voronova, N., Nigmatullina, L., Kuznetsova, E., Timonina, V., Efimenko, B., Turgunkhujaev, O., Avdeichik, S., Ansar, M., Popadin, K. Y., et al. (2023) · Genes · doi:10.3390/genes14030720 · Cited by 1

Molecular Diagnosis of Genetic Diseases of the Kidney: Primer for Pediatric Nephrologists

Waters, A. M., & Lemaire, M. J. (2023) · Springer eBooks · doi:10.1007/978-3-031-11665-0_4 · Cited by 1

Youth consanguinity in relation to sociodemographic and women-related fertility factors in the Arab society of Israel

Zalan, A. A., Khatib, M. N., Sheikh-Muhammad, A. A., Mahajnah, M. M., & Sharkia, R. A. (2023) · World Journal of Advanced Research and Reviews · doi:10.30574/wjarr.2023.19.3.1836 · Cited by 1

Comprehensive program development for congenital heart disease in the United Arab Emirates and in Singapore

Király, L., Aye, M. M. W., Subbian, S. K., Shah, N., Hetharsi, B., Hakami, A. A., & Kofidis, T. (2023) · Journal of Humanitarian Cardio Vascular Medicine · doi:10.12681/jhcvm.34673 · Cited by 1

Knowledge and Attitudes Toward Premarital Screening Programs Among Students at the University of Tripoli, Libya

Shebani, A., Mustafa, A. M., Elshwekh, H., Hmmier, A., & Alhudiri, I. M. (2024) · Cureus · doi:10.7759/cureus.64274 · Cited by 1

Death Causes Among Iranian Children With Leukodystrophies

Shiva, M., Hosseinpour, S., Ashrafi, M. R., Heidari, M., Rezaei, Z., Zebardast, J., Mohammadpour, M., Bonkowsky, J. L., & Tavasoli, A. R. (2024) · Journal of Child Neurology · doi:10.1177/08830738241293171 · Cited by 1

Consanguinity and rare monogenic systemic autoinflammatory disorders: implications for prevalence and genetic variability

AlSaleem, A., & Al-Mayouf, S. M. (2025) · Pediatric Rheumatology · doi:10.1186/s12969-025-01133-z · Cited by 1

Precision Medicine of Rare Genetic Diseases in Africa

Romdhane, L., Mezzi, N., El‐Kamah, G. Y., Abdelhak, S., & Kumuthini, J. (2025) · Springer eBooks · doi:10.1007/978-981-96-8959-0_7 · Cited by 1

Quantitative fluorescent‐polymerase chain reaction: First line investigation for trisomy 21 in a developing country

Gulati, R., Muthuswamy, S., Bhat, V. B., & Agarwal, S. (2014) · Journal of Paediatrics and Child Health · doi:10.1111/jpc.12687 · Cited by 1

BRCA1 genetic testing in a Pakistani breast‐ovarian cancer family with multiple consanguineous marriages

Rashid, M. U., Muhammad, N., Iqbal, K., Yusuf, H., & Hamann, U. (2014) · Clinical Genetics · doi:10.1111/cge.12533 · Cited by 1

Multidisciplinary management of Papillon-Lefevre syndrome as a result of consanguineous marriage

Ramkumar, N., & Sankar, H. (2022) · BMJ Case Reports · doi:10.1136/bcr-2022-252992 · Cited by 1

The practice of consanguineous marriage and the risk of diabetes among offspring in the province of Tetouan (Morocco)

Hajjaji, M., Khadmaoui, A., & Bakkali, M. E. (2023) · Arab Gulf Journal of Scientific Research · doi:10.1108/agjsr-08-2022-0134 · Cited by 2

Pattern of fetal congenital anomalies among consanguineous marriages in Cairo University Hospitals

Gaafar, H. M., Hamid, A. A. A. E., Ismail, G. M., & Eswi, A. (2014) · Evidence Based Women s Health Journal · doi:10.1097/01.ebx.0000452876.69144.04 · Cited by 1

Biochemical study of glycogen storage disease type II (Pompe disease) in Egyptian infants

Fateen, E., Hamza, H., Matty, D. M. A.-E., Gouda, A. S., El-Saiedi, S. A., Saleh, S. M., Elfeel, N. M. S., & Ismail, M. A. Y. (2017) · Middle East Journal of Medical Genetics · doi:10.1097/01.mxe.0000521019.02657.75 · Cited by 1

The Effectiveness of Thalassemia Control Measures in the United Arab Emirates

Dhaheri, H. A., & Kim, S. (2018) · International Conference on Control, Artificial Intelligence, Robotics & Optimization (ICCAIRO) · doi:10.1109/iccairo.2018.00020 · Cited by 1

The demographic data and the high frequency of chromosome/chromatid breaks as biomarkers for genome integrity have a role in predicting the susceptibility to have Down syndrome in a cohort of Egyptian young-aged mothers

El-Attar, L. M., Issa, N. M., & Mahrous, H. (2019) · Egyptian Journal of Medical Human Genetics · doi:10.1186/s43042-019-0020-7 · Cited by 1

Population Structure of a Remnant Quilombo Community: An Analysis of the Inbreeding and Ethnic Admixture

Cruz, J. D. O., Lima, P., & Sousa, S. M. B. (2020) · OALib · doi:10.4236/oalib.1106207 · Cited by 1

Prevalence and Risk Factors of Consanguineous Marriage

Heidari, F., & Dastgiri, S. (2014) · DergiPark (Istanbul University) · Cited by 1

Exome‐based preconception carrier testing for consanguineous couples in China

He, Y., Xie, R., Lou, J., Li, Y., Wang, C., Zhang, V. W., & Li, D. (2021) · Prenatal Diagnosis · doi:10.1002/pd.6018 · Cited by 1

Prenatal diagnosis of congenital fetal malformations medically terminated: a retrospective analysis

Dasari, P., & Aggrawal, P. (2021) · The New Indian Journal of OBGYN · doi:10.21276/obgyn.2021.8.1.13 · Cited by 1

Evaluation of triple hormonal content (ER, PR, and HER\2neu)of breast cancer specimens obtained from breast cancer patients using tru-cut biopsy

Jasim, M. H., Akool, M. A.-Z., & Al-Obaidi, S. M. (2016) · Journal of the Faculty of Medicine Baghdad · doi:10.32007/jfacmedbagdad.583248 · Cited by 1

Glycogen storage disease in two sisters: A case report

Twanabasu, S., Duwadee, P., Homagain, S., Ghimire, J., & Rijal, R. C. (2023) · Clinical Case Reports · doi:10.1002/ccr3.7318 · Cited by 1

The Role of Consanguineous Marriages in the Development of Intellectual DisabilitiesPreprint

Aliyeva, Z., Preis, E., & Jacob, T. (2022) · Research Square · doi:10.21203/rs.3.rs-1573754/v1 · Cited by 1

Consanguinity in the Lebanese Population: Knowledge, Attitude and PracticePreprint

Chouery, É., Ibrahim, J.-N., Deeb, M. E., Sobh, A., Ghanem, M., Sobh, J., Choueiry, F. E., Rashwan, R., Swaidan, D., Abdelrazzak, A., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-4538121/v1 · Cited by 1

Education and Consanguineous Marriage

Akyol, P., & Mocan, N. H. (2022) · Journal of Human Capital · doi:10.1086/723092

Genetic Testing, Interpretation of Genetic Test Reports and Genetic Counseling for Clinicians

Bennett, R. L. (2015) · Springer eBooks · doi:10.1007/978-3-319-17223-1_19

Microarray abnormal results

Zneimer, S. M. (2014) · doi:10.1002/9781118412602.ch17

De l’intérêt de partenariats autour du bassin méditerranéen pour les maladies rares

Mégarbané, A. (2012) · La Presse Médicale · doi:10.1016/j.lpm.2012.02.033

Do Marital Habits Affect Epilepsy Classifications and Etiologies? Update from Epilepsy Registry

Babtain, F. A., & Arabia, S. (2014) · American Journal of Medicine and Medical Sciences

Genetic Counselling: Consanguinity and Cultural Expectations

Karbani, G. (2012) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0006179.pub2

Everyone is unique: Dealing with diversity in genetic counselling

Mountain, H. (2015) · Murdoch University Research Portal

Clinical utility of next-generation sequencing in neurodevelopmental disorders: non-syndromic intellectual disability as a model

Çağlayan, A. O. (2015) · Istanbul Bilim University Florence Nightingale Journal of Medicine · doi:10.5606/fng.btd.2015.011

Een Turks echtpaar met een kinderwens

Suurmond, J., Seeleman, C., Stronks, K., & Essink‐Bot, M. (2012) · Bohn Stafleu van Loghum eBooks · doi:10.1007/978-90-313-9147-9_22

Consanguinité et prédisposition génétique à l’épilepsie

Chentouf, A. (2015) · European Psychiatry · doi:10.1016/j.eurpsy.2015.09.374

Study of Congenital Anomalies Associated with a Consanguineous Married Couple

Dehankar, R., Bhakare, U., Paikrao, V. M., & Ksheersagar, D. D. (2016) · International Journal of Medical Research Professionals · doi:10.21276/ijmrp.2016.2.5.045

Consanguinity and counseling consanguineous couples

Hamamy, H. (2016) · Geneva Foundation for Medical Education and Research

Genetic Diagnosis of Renal Diseases: Basic Concepts and Testing

Waters, A. M., & Lemaire, M. J. (2016) · Springer eBooks · doi:10.1007/978-3-662-52972-0_4

Infective Causes of Epilepsy

Krishnamoorthy, E. S., Shorvon, S. D., & Schachter, S. C. (2017) · Epilepsy · doi:10.1017/9781139547918.002

SNP arrays na detecção de alterações estruturais e no número de cópias em pacientes portadores de deficiência intelectual idiopática

dos Santos, A. (2017) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.41.2017.tde-12072017-082102

Exome sequencing analysis of rare autosomal recessive disorders

Alsaedi, A. (2017) · University of Birmingham Institutional Research Archive (University of Birmingham)

Interrogating heterosis and consanguinity for livestock and human populations

Aneni, M. O., & Antigha, E. (2018) · AFRREV STECH An International Journal of Science and Technology · doi:10.4314/stech.v7i2.3

Evaluation of triple hormonal content (ER, PR, and HER\2neu)of breast cancer specimens obtained from breast cancer patients using tru-cut biopsy

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