reference/17170071

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17170071

Outgoing Links

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endingPage	29
issn	1061-4036 1546-1718
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publicationName	Nature Genetics
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bibliographicCitation	Li QY, Newbury-Ecob RA, Terrett JA, Wilson DI, Curtis AR, Yi CH, Gebuhr T, Bullen PJ, Robson SC, Strachan T, Bonnet D, Lyonnet S, Young ID, Raeburn JA, Buckler AJ, Law DJ, Brook JD. Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family. Nat Genet. 1997 Jan;15(1):21–9. doi: 10.1038/ng0197-21. PMID: 8988164.
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date	199701
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/ https://www.crossref.org/
title	Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family
discusses	http://id.nlm.nih.gov/mesh/M0019167 http://id.nlm.nih.gov/mesh/M0006678 http://id.nlm.nih.gov/mesh/M0328076 http://id.nlm.nih.gov/mesh/M0021788 http://id.nlm.nih.gov/mesh/M0204396 http://id.nlm.nih.gov/mesh/M0008410 http://id.nlm.nih.gov/mesh/M0269845 http://id.nlm.nih.gov/mesh/M0006644
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Incoming Links

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Total number of triples: 59.