A Novel SRD5A2 Mutation with Loss of Function Identified in Chinese Patients with Hypospadias

Publisher： Karger

E-ISSN： 1663-2826|76|1|44-49

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.76, Iss.1, 2011-05, pp. : 44-49

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

Clinical Characterization and Analysis of the SRD5A2 Gene in Six Korean Patients with 5α-Reductase Type 2 Deficiency

By  

Hormone Research in Paediatrics, Vol. 73, Iss. 1, 2010-01 ,pp. : 41-48

Karger

Access to resources Recommend Favorite

A Novel Mutation in the TBG Gene Producing Partial Thyroxine-Binding Globulin Deficiency (Glencoe) Identified in 2 Families

By  

European Thyroid Journal, Vol. 6, Iss. 3, 2017-02 ,pp. : 138-142

Karger

Access to resources Recommend Favorite

Hearing Loss Is Part of the Clinical Picture of ENPP1 Loss of Function Mutation

By  

Hormone Research in Paediatrics, Vol. 81, Iss. 1, 2013-11 ,pp. : 63-66

Karger

Access to resources Recommend Favorite

Steroid 5α-Reductase 1 Polymorphisms and Testosterone/Dihydrotestosterone Ratio in Male Patients with Hypospadias

By  

Hormone Research in Paediatrics, Vol. 61, Iss. 4, 2004-03 ,pp. : 180-183

Karger

Access to resources Recommend Favorite

Loss-of-Function SOX10 Mutation in a Patient with Kallmann Syndrome, Hearing Loss, and Iris Hypopigmentation

By  

Hormone Research in Paediatrics, Vol. 84, Iss. 3, 2015-07 ,pp. : 212-216

Karger

Access to resources Recommend Favorite