Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene-Reference-Cited by-同舟云学术

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Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene

Published:2003-05-01 Issue:5 Volume:40 Page:53e-53
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:
Short-container-title:

Author:

Koppens P F J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 14 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. EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency;European Journal of Human Genetics;2020-07-02

2. Szteroid-21-hidroxiláz-deficientia, a congenitalis adrenalis hyperplasia leggyakoribb oka;Orvosi Hetilap;2018-02

3. Human Cytochrome P450 Enzymes;Cytochrome P450;2015

4. Common Genetic Variants of the Human Steroid 21-Hydroxylase Gene (CYP21A2) Are Related to Differences in Circulating Hormone Levels;PLoS ONE;2014-09-11

5. Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene;Genome Biology and Evolution;2012-12-12

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