reference/11947517

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11947517

Outgoing Links

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contentType	Comparative Study\|Journal Article\|Research Support, N.I.H., Extramural\|Research Support, Non-U.S. Gov't
endingPage	524
issn	1098-3600
issueIdentifier	7
pageRange	517-524
publicationName	Genetics in medicine : official journal of the American College of Medical Genetics
startingPage	517
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bibliographicCitation	Schimmenti LA, Martinez A, Telatar M, Lai CH, Shapiro N, Fox M, Warman B, McCarra M, Crandall B, Sininger Y, Grody WW, Palmer CG. Infant hearing loss and connexin testing in a diverse population. Genet Med. 2008 Jul;10(7):517–24. doi: 10.1097/gim.0b013e31817708fa. PMID: 18580690.
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date	200807
identifier	https://pubmed.ncbi.nlm.nih.gov/18580690 https://doi.org/10.1097/gim.0b013e31817708fa
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Infant hearing loss and connexin testing in a diverse population
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Total number of triples: 62.