A missense mutation in the second transmembrane segment of the luteinizing hormone receptor causes familial male-limited precocious puberty
Publication year
1995Source
Journal of Clinical Endocrinology and Metabolism, 80, 11, (1995), pp. 3168-3172ISSN
Publication type
Article / Letter to editor

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Organization
Otorhinolaryngology
Human Genetics
Journal title
Journal of Clinical Endocrinology and Metabolism
Volume
vol. 80
Issue
iss. 11
Page start
p. 3168
Page end
p. 3172
Subject
Clinical description and delineation of genetic syndromes; Klinische beschrijving en moleculaire definiëring van genetische syndromenThis item appears in the following Collection(s)
- Academic publications [234412]
- Faculty of Medical Sciences [89250]
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