Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development

Author:

Mazen Inas1,Mekkawy Mona2ORCID,Kamel Alaa2,Essawi Mona3,Hassan Heba3ORCID,Abdel‐Hamid Mohamed3ORCID,Amr Khalda3ORCID,Soliman Hala3,El‐Ruby Mona1,Torky Ahmed1,El Gammal Mona1,Elaidy Aya1,Bashamboo Anu4,McElreavey Kenneth4

Affiliation:

1. Department of Clinical Genetics National Research Centre Cairo Egypt

2. Department of Human Cytogenetics National Research Center Cairo Egypt

3. Department of Medical Molecular Genetics National Research Centre Cairo Egypt

4. Developmental Genetics and Stem Cell Biology Institut Pasteur Paris France

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference64 articles.

1. Ambiguous genitalia: Medical, socio‐cultural and religious factors affecting management in Saudi Arabia;Abdullah M. A.;Annals of Tropical Paediatrics,1991

2. The most encountered groups of genetic disorders in Giza Governorate, Egypt;Afifi H. H.;Bratislavské Lekárske Listy,2010

3. International networks for supporting research and clinical care in the field of disorders of sex development;Ahmed S. F.;Endocrine Development,2014

4. Genotype‐phenotype analysis of pediatric patients with WT1 glomerulopathy;Ahn Y. H.;Pediatric Nephrology,2017

5. AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity;Akcay T.;Andrology,2014

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