A novelSRD5A2mutation in an Iranian family with sex development disorder-Reference-Cited by-同舟云学术

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A novelSRD5A2mutation in an Iranian family with sex development disorder

Published:2020-10-25 Issue:1 Volume:53 Page:
ISSN:0303-4569
Container-title:Andrologia
language:en
Short-container-title:Andrologia

Author:

Hashemi‐Gorji Feyzollah¹^ORCID,Salehpour Shadab²,Miryounesi Mohammad¹,Mirfakhraie Reza¹³^ORCID,Yassaee Vahid Reza¹³

Affiliation:

1. Genomic Research Center Shahid Beheshti University of Medical Sciences Tehran Iran

2. Department of Pediatrics Faculty of Medicine Shahid Beheshti University of Medical Sciences Tehran Iran

3. Department of Medical Genetics Faculty of Medicine Shahid Beheshti University of Medical Sciences Tehran Iran

Publisher

Wiley

Subject

Urology,Endocrinology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/and.13847

Reference30 articles.

1. Disorders of sex development: effect of molecular diagnostics

2. Molecular investigation of mutations in androgen receptor and 5‐alpha‐reductase‐2 genes in 46,XY Disorders of Sex Development with normal testicular development

3. Phenotypic Features, Androgen Receptor Binding, and Mutational Analysis in 278 Clinical Cases Reported as Androgen Insensitivity Syndrome

4. 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’

5. Update on the genetics of differences of sex development (DSD)

Cited by 1 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. The Molecular Basis of 5α-Reductase Type 2 Deficiency;Sexual Development;2022

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