A Novel SRY Mutation Leads to Asymmetric SOX9 Activation and Is Responsible for Mixed 46,XY Gonadal Dysgenesis

Publisher： Karger

E-ISSN： 1663-2826|78|3|188-192

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.78, Iss.3, 2012-03, pp. : 188-192

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants

By  

Hormone Research in Paediatrics, Vol. 75, Iss. 1, 2010-08 ,pp. : 26-31

Karger

Access to resources Recommend Favorite

Management of Males with 45,X/46,XY Gonadal Dysgenesis

By  

Hormone Research in Paediatrics, Vol. 52, Iss. 1, 2000-01 ,pp. : 11-14

Karger

Access to resources Recommend Favorite

Preserved Fertility in a Patient with a 46,XY Disorder of Sex Development due to a New Heterozygous Mutation in the NR5A1/SF-1 Gene: Evidence of 46,XY and 46,XX Gonadal Dysgenesis Phenotype Variability in Multiple Members of an Affected Kindred

By  

Hormone Research in Paediatrics, Vol. 78, Iss. 2, 2012-08 ,pp. : 119-126

Karger

Access to resources Recommend Favorite

WT1 Deletion Leading to Severe 46,XY Gonadal Dysgenesis, Wilms Tumor and Gonadoblastoma: Case Report

By  

Hormone Research in Paediatrics, Vol. 83, Iss. 3, 2015-01 ,pp. : 211-216

Karger

Access to resources Recommend Favorite

Mixed Gonadal Dysgenesis and Precocious Puberty

By  

Hormone Research in Paediatrics, Vol. 58, Iss. 1, 2002-08 ,pp. : 30-33

Karger

Access to resources Recommend Favorite