reference/11844531

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11844531

Outgoing Links

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publicationName	Journal of pediatric endocrinology & metabolism : JPEM
startingPage	1041
bibliographicCitation	Quinteiro C, Castro-Feijoo L, Loidi L, Barreiro J, de la Fuente M, Dominguez F, Pombo M. Novel mutation involving the translation initiation codon of the growth hormone receptor gene (GHR) in a patient with Laron syndrome. J Pediatr Endocrinol Metab. 2002 Jul;15(7):1041–5. doi: 10.1515/jpem.2002.15.7.1041. PMID: 12199334.
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date	200201
identifier	https://doi.org/10.1515/jpem.2002.15.7.1041 https://pubmed.ncbi.nlm.nih.gov/12199334
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Novel Mutation Involving the Translation Initiation Codon of the Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome
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Total number of triples: 57.