Primary amenorrhoea with hypertension: undiagnosed 17‐α‐hydroxylase deficiency-Reference-Cited by-同舟云学术

Primary amenorrhoea with hypertension: undiagnosed 17‐α‐hydroxylase deficiency

Published:2013-10 Issue:8 Volume:199 Page:556-558
ISSN:0025-729X
Container-title:Medical Journal of Australia
language:en
Short-container-title:Medical Journal of Australia

Author:

Britten Fiona L¹,Ulett Kimberly B¹,Duncan Emma L¹,Perry‐Keene Donald A¹

Affiliation:

1. Royal Brisbane and Women's Hospital, Brisbane, QLD.

Publisher

AMPCo

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.5694/mja12.11619

Reference15 articles.

1. Steroid 17α-hydroxylase deficiency: First Australian case report

2. Genetic analysis of the cytochrome P-450c17α (CYP17) and aldosterone synthase (CYP11B2) in Japanese patients with 17α-hydroxylase deficiency

3. KaterCE.The 17‐alpha and 11‐beta hydroxylase deficiency forms of congenital adrenal hyperplasia.Presentation at ENDO 2011 (The Endocrine Society's 93rd Annual Meeting); 2011 Jun 4‐7; Boston USA.

4. Human Gene Mutation Database [internet database].Institute of Medical Genetics Cardiff University.http://www.hgmd.cf.ac.uk/ac/index.php(accessed Sep 2012).

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

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