Genotyping of a Chinese family with 46,XX and 46,XY 17-hydroxylase deficiency-Reference-Cited by-同舟云学术

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Genotyping of a Chinese family with 46,XX and 46,XY 17-hydroxylase deficiency

Published:2009-01 Issue:8 Volume:25 Page:485-490
ISSN:0951-3590
Container-title:Gynecological Endocrinology
language:en
Short-container-title:Gynecological Endocrinology

Author:

Tian Qinjie,Yao Fengxia,Sha Guihua,Huang Shangzhi,Tseng Hung,Schindler Adolf E.

Publisher

Informa UK Limited

Subject

Obstetrics and Gynaecology,Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.tandfonline.com/doi/pdf/10.1080/09513590902898239

Reference15 articles.

1. Canadian Mennonites and individuals residing in the Friesland region of the Netherlands share the same molecular basis of 17?-hydroxylase deficiency

2. Phenotype-Genotype Correlation in Eight Chinese 17α-Hydroxylase/17,20 Lyase-Deficiency Patients with Five Novel Mutations of CYP17A1 Gene

3. MutScreener: primer design tool for PCR-direct sequencing

Cited by 15 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 mutations of the CYP17A1 gene cause disorders of sex development in two-chromosome karyotype 46,XY infants and a literature review: A case report;2023-11-29

2. Ovarian gonadoblastoma with dysgerminoma in a girl with 46,XX karyotype 17a-hydroxylase/17, 20-lyase deficiency: A case report and literature review;Frontiers in Endocrinology;2022-12-15

3. 17 alpha‐hydroxylase deficiency: A case report of young Chinese woman with a rare gene mutation;Clinical Case Reports;2022-07

4. 46,XX DSD;Disorders|Differences of Sex Development;2020

5. Prevalence of CYP17A1 gene mutations in 17α-hydroxylase deficiency in the Chinese Han population;Clinical Hypertension;2019-10-15

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