reference/31177608

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/31177608

Outgoing Links

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contentType	Journal Article
endingPage	636
issn	2359-3997 2359-4292
issueIdentifier	6
pageRange	633-636
publicationName	Archives of Endocrinology and Metabolism
startingPage	633
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bibliographicCitation	Correa FA, França MM, Fang Q, Ma Q, Bachega TA, Rodrigues A, Ozel BA, Li JZ, Mendonca BB, Jorge AAL, Carvalho LR, Camper SA, Arnhold IJP. Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing. Arch. Endocrinol. Metab. 2017 Dec;61(6):633–6. doi: 10.1590/2359-3997000000311.
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date	201712
identifier	https://pubmed.ncbi.nlm.nih.gov/29412390 https://pubmed.ncbi.nlm.nih.gov/PMC5806044 https://doi.org/10.1590/2359-3997000000311
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing
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Total number of triples: 70.