KAL1 mutations are not a common cause of idiopathic hypogonadotrophic hypogonadism in humans-Reference-Cited by-同舟云学术

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KAL1 mutations are not a common cause of idiopathic hypogonadotrophic hypogonadism in humans

Published:2007-01-09 Issue:3 Volume:13 Page:165-170*
ISSN:1360-9947
Container-title:MHR: Basic science of reproductive medicine
language:en
Short-container-title:

Author:

Bhagavath Balasubramanian,Xu Ning,Ozata Metin,Rosenfield Robert L.,Bick David P.,Sherins Richard J.,Layman Lawrence C.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Obstetrics and Gynaecology,Genetics,Molecular Biology,Embryology,Reproductive Medicine

Link

http://academic.oup.com/molehr/article-pdf/13/3/165/6389038/gal108.pdf

Reference49 articles.

1. Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2);Albuisson;Hum Mutat,2005

2. The prevalence of gonadotropin-releasing hormone receptor mutations in a large cohort of patients with hypogonadotropic hypogonadism;Bhagavath;Fertil Steril,2005

3. Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism;Bhagavath;Fertil Steril,2006

4. Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome;Bick;N Engl J Med,1992

5. Deletion analysis maps ocular albinism proximal to the steroid sulphatase locus;Bouloux;Clin Genet,1993

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1. Prevalence of pathogenic variants and digenic disease in patients diagnosed with normosmic hypogonadotropic hypogonadism/Kallmann Syndrome;Molecular and Cellular Endocrinology;2024-08

2. Facing the Challenge: Hormonal hurdles, Olfaction Obstacles in Kallmann Syndrome;Research Journal of Pharmacology and Pharmacodynamics;2023-11-09

3. X-linked recessive Kallmann syndrome: A case report;World Journal of Clinical Cases;2022-09-06

4. Clinical data and genetic mutation in Kallmann syndrome with CHARGE syndrome;Medicine;2018-07

5. Role of Kisspeptine in Regulation of Reproductive Function;Journal of obstetrics and women's diseases;2016-12-15

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