Homozygous Mutation of the <b><i>FGFR1</i></b> Gene Associated with Congenital Heart Disease and 46,XY Disorder of Sex Development-Reference-Cited by-同舟云学术

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Homozygous Mutation of the FGFR1 Gene Associated with Congenital Heart Disease and 46,XY Disorder of Sex Development

Published:2016-04-08 Issue:1 Volume:10 Page:16-22
ISSN:1661-5425
Container-title:Sexual Development
language:en
Short-container-title:Sex Dev

Author:

Mazen Inas,Amin Heba,Kamel Alaa,El Ruby Mona,Bignon-Topalovic Joelle,Bashamboo Anu,McElreavey Ken

Publisher

S. Karger AG

Subject

Developmental Biology,Embryology,Endocrinology, Diabetes and Metabolism

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Bart's syndrome associated with a disorder of sexual differentiation: An atypical presentation in a Cameroonian newborn;Clinical Case Reports;2022-01

2. Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development;American Journal of Medical Genetics Part A;2021-03-19

3. Understanding Heart Field Progenitor Cells for Modeling Congenital Heart Diseases;Current Cardiology Reports;2021-03-11

4. Disorders of Sex Development: New Concepts of Diagnostics and Management in Children;Педиатрия. Восточная Европа;2020-07-24

5. GENETICS IN ENDOCRINOLOGY: Approaches to molecular genetic diagnosis in the management of differences/disorders of sex development (DSD): position paper of EU COST Action BM 1303 ‘DSDnet’;European Journal of Endocrinology;2018-10

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