Female-to-male sex reversal associated with unique Xp21.2 deletion disrupting genomic regulatory architecture of the dosage-sensitive sex reversal region-Reference-Cited by-同舟云学术

Female-to-male sex reversal associated with unique Xp21.2 deletion disrupting genomic regulatory architecture of the dosage-sensitive sex reversal region

Published:2017-05-08 Issue:10 Volume:54 Page:705-709
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Dangle Pankaj,Touzon María Sol,Reyes-Múgica Miguel,Witchel Selma F,Rajkovic Aleksandar,Schneck Francis X,Yatsenko Svetlana A

Funder

National Institute of Child Health and Human Development

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference20 articles.

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3. Perspectives in Pediatric Pathology, Chapter 7. ovotesticular DSD (True hermaphroditism);Nistal;Pediatr Dev Pathol,2015

4. A SOX9 duplication and familial 46,XX developmental testicular disorder;Cox;N Engl J Med,2011

5. Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex development;Kim;J Med Genet,2015

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