The Clinical and Molecular Heterogeneity of 17βHSD-3 Enzyme Deficiency

Publisher： Karger

E-ISSN： 1663-2826|74|4|229-240

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.74, Iss.4, 2010-08, pp. : 229-240

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

A Single Nucleotide Variant in the Promoter Region of 17β-HSD Type 5 Gene Influences External Genitalia Virilization in Females with 21-Hydroxylase Deficiency

By  

Hormone Research in Paediatrics, Vol. 85, Iss. 5, 2016-04 ,pp. : 333-338

Karger

Access to resources Recommend Favorite

Clinical, Endocrine, and Molecular Genetic Findings in Patients with 17β-Hydroxysteroid Dehydrogenase Deficiency

By  

Hormone Research in Paediatrics, Vol. 53, Iss. 1, 2000-08 ,pp. : 26-31

Karger

Access to resources Recommend Favorite

A Case of 3β-Hydroxysteroid Dehydrogenase Type II (HSD3B2) Deficiency Picked up by Neonatal Screening for 21-Hydroxylase Deficiency: Difficulties and Delay in Etiologic Diagnosis

By  

Hormone Research in Paediatrics, Vol. 68, Iss. 4, 2007-05 ,pp. : 204-208

Karger

Access to resources Recommend Favorite

A Novel Homozygous Q334X Mutation in the HSD3B2 Gene Causing Classic 3β-Hydroxysteroid Dehydrogenase Deficiency: An Unexpected Diagnosis after a Positive Newborn Screen for 21-Hydroxylase Deficiency

By  

Hormone Research in Paediatrics, Vol. 77, Iss. 5, 2012-02 ,pp. : 334-338

Karger

Access to resources Recommend Favorite

The Expression of Omental 11β-HSD1 Is Not Increased in Severely Obese Women with Metabolic Syndrome

By  

Obesity Facts, Vol. 5, Iss. 1, 2012-03 ,pp. : 104-111

Karger

Access to resources Recommend Favorite