reference/14687922

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14687922

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endingPage	2276
issn	1460-2083 0964-6906
issueIdentifier	12
pageRange	2266-2276
publicationName	Human Molecular Genetics
startingPage	2266
bibliographicCitation	Carré A, Szinnai G, Castanet M, Sura-Trueba S, Tron E, Broutin-L'Hermite I, Barat P, Goizet C, Lacombe D, Moutard ML, Raybaud C, Raynaud-Ravni C, Romana S, Ythier H, Léger J, Polak M. Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case. Hum Mol Genet. 2009 Jun 15;18(12):2266–76. doi: 10.1093/hmg/ddp162. PMID: 19336474.
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date	2009-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1093/hmg/ddp162 https://pubmed.ncbi.nlm.nih.gov/19336474
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case
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