Clinical characteristics and follow-up of 5 young Chinese males with gonadotropin-releasing hormone deficiency caused by mutations in the KAL1 gene-Reference-Cited by-同舟云学术

Clinical characteristics and follow-up of 5 young Chinese males with gonadotropin-releasing hormone deficiency caused by mutations in the KAL1 gene

Published:2016-02 Issue: Volume:7 Page:64-69
ISSN:2214-5400
Container-title:Meta Gene
language:en
Short-container-title:Meta Gene

Author:

Li Juan,Li Niu,Ding Yu,Huang Xiaodong,Shen Yongnian,Wang Jian,Wang Xiumin

Funder

Shanghai Municipal Science and Technology Commission

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference15 articles.

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2. Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypes;Costa-Barbosa;J. Clin. Endocrinol. Metab.,2013

3. Normosmic idiopathic hypogonadotropic hypogonadism: update on the genetic background and future challenges;Fathi;J. Pediatr. Endocrinol. Metab.,2013

4. Congenital hypogonadotropic hypogonadism and Kallmann syndrome in males;Ghervan;Presse Med.,2014

5. A window of opportunity: the diagnosis of gonadotropin deficiency in the male infant;Grumbach;J. Clin. Endocrinol. Metab.,2005

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