reference/14597796

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14597796

Outgoing Links

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contentType	Case Reports\|Letter
endingPage	534
issn	0300-0664 1365-2265
issueIdentifier	4
pageRange	533-534
publicationName	Clinical Endocrinology
startingPage	533
bibliographicCitation	Latronico AC, Billerbeck AE, Pinto EM, Brazil D'Alva C, Arnhold IJ, Mendonca BB. Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocious puberty. Clin Endocrinol (Oxf). 2003 Oct;59(4):533–4. doi: 10.1046/j.1365-2265.2003.01810.x. PMID: 14510919.
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date	2003-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/14510919 https://doi.org/10.1046/j.1365-2265.2003.01810.x
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male‐limited precocious puberty
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Total number of triples: 37.