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Genetic causes of human reproductive disease

Achermann, JC; Ozisik, G; Meeks, JJ; Jameson, JL; (2002) Genetic causes of human reproductive disease. The Journal of Clinical Endocrinology & Metabolism , 87 (6) 2447 - 2454. 10.1210/jc.87.6.2447. Green open access

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Type: Article
Title: Genetic causes of human reproductive disease
Open access status: An open access version is available from UCL Discovery
DOI: 10.1210/jc.87.6.2447
Publisher version: http://dx.doi.org/10.1210/jc.87.6.2447
Language: English
Additional information: © 2002 by The Endocrine Society This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/us/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: FOLLICLE-STIMULATING-HORMONE, STEROIDOGENIC FACTOR-I, IDIOPATHIC HYPOGONADOTROPIC HYPOGONADISM, ADRENAL HYPOPLASIA CONGENITA, LINKED KALLMANN-SYNDROME, SEPTO-OPTIC DYSPLASIA, RECEPTOR GENE, BETA-SUBUNIT, LUTEINIZING-HORMONE, SEX REVERSAL
UCL classification: UCL
UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health > Genetics and Genomic Medicine Dept
URI: https://discovery.ucl.ac.uk/id/eprint/113451
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