reference/17300465

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17300465

Outgoing Links

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contentType	Case Reports\|Journal Article\|Research Support, Non-U.S. Gov't
endingPage	193
issn	0022-3476
issueIdentifier	2
pageRange	190-193
publicationName	The Journal of Pediatrics
startingPage	190
bibliographicCitation	Doyle DA, Gonzalez I, Thomas B, Scavina M. Autosomal dominant transmission of congenital hypothyroidism, neonatal respiratory distress, and ataxia caused by a mutation of NKX2-1. The Journal of Pediatrics. 2004 Aug;145(2):190–3. doi: 10.1016/j.jpeds.2004.04.011.
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date	200408
identifier	https://doi.org/10.1016/j.jpeds.2004.04.011 https://pubmed.ncbi.nlm.nih.gov/15289765
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/5127 https://portal.issn.org/resource/ISSN/0022-3476
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Autosomal dominant transmission of congenital hypothyroidism, neonatal respiratory distress, and ataxia caused by a mutation of NKX2-1
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Incoming Links

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Total number of triples: 45.