Clinical and genetic analysis for two Chinese siblings with 17α-hydroxylase/17,20-lyase deficiency-Reference-Cited by-同舟云学术

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Clinical and genetic analysis for two Chinese siblings with 17α-hydroxylase/17,20-lyase deficiency

Published:2011-11-21 Issue:6 Volume:28 Page:455-459
ISSN:0951-3590
Container-title:Gynecological Endocrinology
language:en
Short-container-title:Gynecological Endocrinology

Author:

Zhou Qi,Wu Chaoming,Wang Liang,Zheng Jingchen,Zheng Chao,Jin Jian,Qian Yanying,Ni Li

Publisher

Informa UK Limited

Subject

Obstetrics and Gynecology,Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.tandfonline.com/doi/pdf/10.3109/09513590.2011.633648

Reference18 articles.

1. 17-hydroxylation deficiency in man.

2. Inborn errors of adrenal steroidogenesis

3. THE GENETICS, PATHOPHYSIOLOGX, AND MANAGEMENT OF HUMAN DEFICIENCIES OF P450c17

4. Regional Mapping of Genes Encoding Human Steroidogenic Enzymes: P450scc to 15q23–q24, Adrenodoxin to 11q22; Adrenodoxin Reductase to 17q24–q25; and P450c17 to 10q24–q25

5. Structural Characterization of Normal and Mutant Human Steroid 17α- Hydroxylase Genes: Molecular Basis of One Example of Combined 17α- Hydroxylase/17,20 Lyase Deficiency

Cited by 6 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. Successful live birth in women with partial 17α-hydroxylase deficiency: report of two cases;Reproductive BioMedicine Online;2024-08

2. Successful live birth in women with partial 17α hydroxylase deficiency: report of two cases;2023-03-09

3. Disorders of sexual development;Handbook of Diagnostic Endocrinology;2021

4. A novel CYP 17 A 1 deletion causes a functional knockout of the steroid enzyme 17‐hydroxylase and 17,20‐lyase in a T urkish family and illustrates the precise role of the CYP 17 A 1 gene;Clinical Case Reports;2015-08-26

5. Clinical and genetic analyses of a Chinese female with 17α-hydroxylase/17,20-lyase deficiency;Gynecological Endocrinology;2014-07-16

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