Analysis of four common salt-wasting mutations in CYP21 (steroid 21-hydroxylase) by cleavase fragment length polymorphism analysis and characterization of a frequent polymorphism in intron 6-Reference-Cited by-同舟云学术

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Analysis of four common salt-wasting mutations in CYP21 (steroid 21-hydroxylase) by cleavase fragment length polymorphism analysis and characterization of a frequent polymorphism in intron 6

Published:1998-09 Issue:3 Volume:3 Page:171-178
ISSN:1084-8592
Container-title:Molecular Diagnosis
language:en
Short-container-title:Molecular Diagnosis

Author:

WEI W,KILLEEN A

Publisher

Elsevier BV

Subject

General Medicine

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency;Genetic Steroid Disorders;2023

2. Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency;Genetic Steroid Disorders;2014

3. Vertical Transmission of Chlamydia trachomatis in Chongqing China;Current Microbiology;2009-01-03

4. Linkage between I172N mutation, a marker of 21-hydroxylase deficiency, and a single nucleotide polymorphism in Int6 of CYP21B gene: A genetic study of Sardinian family;Clinica Chimica Acta;2006-02

5. Prenatal diagnosis of 21-hydroxylase deficiency caused by gene conversion and rearrangements: pitfalls and molecular diagnostic solutions;Prenatal Diagnosis;2002

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