reference/20002053

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publicationName	Clinical Endocrinology
startingPage	36
bibliographicCitation	Jorge AA, Souza SC, Arnhold IJ, Mendonca BB. The first homozygous mutation (S226I) in the highly-conserved WSXWS-like motif of the GH receptor causing Laron syndrome: supression of GH secretion by GnRH analogue therapy not restored by dihydrotestosterone administration. Clin Endocrinol (Oxf). 2004 Jan;60(1):36–40. doi: 10.1111/j.1365-2265.2004.01930.x. PMID: 14678285.
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date	2003-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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title	The first homozygous mutation (S226I) in the highly‐conserved WSXWS‐like motif of the GH receptor causing Laron syndrome: supression of GH secretion by GnRH analogue therapy not restored by dihydrotestosterone administration
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