Molecular analysis of patient and carrier genes with congenital steroid 21-hydroxylase deficiency by using polymerase chain reaction and single strand conformation polymorphism.-Reference-Cited by-同舟云学术

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Molecular analysis of patient and carrier genes with congenital steroid 21-hydroxylase deficiency by using polymerase chain reaction and single strand conformation polymorphism.

Published:1993-11-01 Issue:5 Volume:92 Page:2182-2190
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Tajima T,Fujieda K,Nakayama K,Fujii-Kuriyama Y

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Cited by 74 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. Novel and Rapid Molecular Diagnosis Methods in Comprehensive Genetic Analysis of 21-hydroxylase Deficiency;2024-04-02

2. Congenital Adrenal Hyperplasia and Human Leukocyte Antigen B: A Meta-Analysis;Cureus;2023-03-08

3. The history of prenatal diagnosis of congenital adrenal hyperplasia;Genetic Steroid Disorders;2023

4. Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision);CLIN PEDIATR ENDOCRI;2022

5. Long-read Amplicon Sequencing of the CYP21A2 in 48 Thai Patients With Steroid 21-Hydroxylase Deficiency;The Journal of Clinical Endocrinology & Metabolism;2022-04-01

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