Clinical Genetic Testing for Kallmann Syndrome-Reference-Cited by-同舟云学术

Clinical Genetic Testing for Kallmann Syndrome

Published:2013-05-01 Issue:5 Volume:98 Page:1860-1862
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Layman Lawrence C.¹

Affiliation:

1. Section of Reproductive Endocrinology, Infertility, and Genetics, Department of Obstetrics and Gynecology, Institute of Molecular Medicine and Genetics, Neuroscience Program, Medical College of Georgia, Georgia Regents University, Augusta, Georgia 30912

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/98/5/1860/9045493/jcem1860.pdf

Reference19 articles.

1. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules;Franco;Nature,1991

2. The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules;Legouis;Cell,1991

3. Intragenic deletion of the KALIG-1 gene in Kallmann's syndrome;Bick;N Engl J Med,1992

4. X Chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene;Hardelin;Proc Natl Acad Sci USA,1992

5. A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor;de Roux;N Engl J Med,1997

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2. Deletion in RMST lncRNA impairs hypothalamic neuronal development in a human stem cell-based model of Kallmann Syndrome;Cell Death Discovery;2024-07-19

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

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5. Nectin-like molecule 2, a necessary sexual maturation regulator, participates in congenital hypogonadotropic hypogonadism;Gene;2020-09