Hypothalamic Dysfunction in a Female with Isolated Hypogonadotropic Hypogonadism and Compound Heterozygous TACR3 Mutations and Clinical Manifestation in Her Heterozygous Mother

Publisher： Karger

E-ISSN： 1663-2826|73|6|477-481

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.73, Iss.6, 2010-04, pp. : 477-481

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

Association between Compound Heterozygous Mutations of SLC34A3 and Hypercalciuria

By  

Hormone Research in Paediatrics, Vol. 82, Iss. 1, 2014-06 ,pp. : 65-71

Karger

Access to resources Recommend Favorite

Central Hypothyroidism Reveals Compound Heterozygous Mutations in the Pit-1 Gene

By  

Hormone Research in Paediatrics, Vol. 49, Iss. 2, 1998-01 ,pp. : 98-102

Karger

Access to resources Recommend Favorite

Clinical, Biochemical and Morphologic Diagnostic Markers in an Infant Male Pseudohermaphrodite Patient with Compound Heterozygous Mutations (G115D/R246W) in SRD5A2 Gene

By  

Hormone Research in Paediatrics, Vol. 62, Iss. 5, 2004-11 ,pp. : 259-264

Karger

Access to resources Recommend Favorite

Compound Heterozygous and Homozygous Mutations of the TSHβ Gene as a Cause of Congenital Central Hypothyroidism in Europe

By  

Hormone Research in Paediatrics, Vol. 62, Iss. 3, 2004-09 ,pp. : 149-155

Karger

Access to resources Recommend Favorite

Genetics of Hypogonadotropic Hypogonadism

By  

Hormone Research in Paediatrics, Vol. 67, Iss. 1, 2007-02 ,pp. : 149-154

Karger

Access to resources Recommend Favorite