46,XX males: a case series based on clinical and genetics evaluation

Author:

Mohammadpour Lashkari F.1,Totonchi M.2,Zamanian M. R.2,Mansouri Z.2,Sadighi Gilani M. A.13,Sabbaghian M.1,Mohseni Meybodi A.2

Affiliation:

1. Department of Andrology; Reproductive Biomedicine Research Center; Royan Institute for Reproductive Biomedicine; ACECR; Tehran Iran

2. Department of Genetics; Reproductive Biomedicine Research Center; Royan Institute for Reproductive Biomedicine; ACECR; Tehran Iran

3. Department of Urology; Shariati Hospital; Tehran University of Medical Sciences; Tehran Iran

Publisher

Wiley

Subject

Urology,Endocrinology,General Medicine

Reference29 articles.

1. Two fast methods for detection of Y-microdeletions;Aknin-Seifer;Fertility and Sterility,2005

2. 46, XX male disorder of sexual development: A case report;Anik;Journal of Clinical Research in Pediatric Endocrinology,2013

3. Genetic evidence equating SRY and the testis-determining factor;Berta;Nature,1990

4. Analytic review: Nature and origin of males with XX sex chromosomes;Chapelle;American Journal of Human Genetics,1972

5. The etiology of XX sex reversal;Chapelle;Reprod Nutr Dev,1990

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