Discordant Genotypic Sex and Phenotype Variations in Two Spanish Siblings with 17α-Hydroxylase/17,20-Lyase Deficiency Carrying the Most Prevalent Mutated<b><i> CYP17A1</i></b> Alleles of Brazilian Patients-Reference-Cited by-同舟云学术

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Discordant Genotypic Sex and Phenotype Variations in Two Spanish Siblings with 17α-Hydroxylase/17,20-Lyase Deficiency Carrying the Most Prevalent Mutated CYP17A1 Alleles of Brazilian Patients

Published:2017 Issue:2 Volume:11 Page:70-77
ISSN:1661-5425
Container-title:Sexual Development
language:en
Short-container-title:Sex Dev

Author:

Fernández-Cancio Mónica,García-García Emilio,González-Cejudo Carmen,Martínez-Maestre María-Angeles,Mangas-Cruz Miguel-Angel,Guerra-Junior Gil,Pandi de Mello Maricilda,Arnhold Ivo J.P.,Nishi Mirian Y.,Bilharinho Mendonça Berenice,García-Arumí Elena,Audí Laura,Tizzano Eduardo,Carrascosa Antonio

Publisher

S. Karger AG

Subject

Developmental Biology,Embryology,Endocrinology, Diabetes and Metabolism

Cited by 7 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. Relationship between dioxins and steroid hormone in 6-year-olds: A follow-up study in an e-waste region of China;Chemosphere;2022-06

4. Mutational Landscape Screening Through Comprehensive In Silico Analysis for Polycystic Ovarian Syndrome–Related Genes;Reproductive Sciences;2021-10-25

5. A report of congenital adrenal hyperplasia due to 17α-hydroxylase deficiency in two 46,XX sisters;Gynecological Endocrinology;2019-08-29

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