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

Publisher： Karger

E-ISSN： 1663-2826|49|2|98-102

ISSN： 1663-2818

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

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

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

Thyroglobulin Gene Mutations in Congenital Hypothyroidism

By  

Hormone Research in Paediatrics, Vol. 75, Iss. 5, 2011-03 ,pp. : 311-321

Karger

Access to resources Recommend Favorite

A New C-Terminal Located Mutation (V272ter) in the PIT-1 Gene Manifesting with Severe Congenital Hypothyroidism

By  

Hormone Research in Paediatrics, Vol. 56, Iss. 3-4, 2002-02 ,pp. : 81-86

Karger

Access to resources Recommend Favorite

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

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

By  

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

Karger

Access to resources Recommend Favorite