reference/25472824

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/25472824

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	493
issn	1432-1203 0340-6717
issueIdentifier	5
pageRange	485-493
publicationName	Human Genetics
startingPage	485
bibliographicCitation	Bartsch O, Schmidt S, Richter M, Morlot S, Seemanová E, Wiebe G, Rasi S. DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein-Taybi syndrome (RSTS) and in another patient with incomplete RSTS. Hum Genet. 2005 Sep;117(5):485–93. doi: 10.1007/s00439-005-1331-y. PMID: 16021471.
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date	2005-07-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1007/s00439-005-1331-y https://pubmed.ncbi.nlm.nih.gov/16021471
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/
title	DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein–Taybi syndrome (RSTS) and in another patient with incomplete RSTS
discusses	http://id.nlm.nih.gov/mesh/M0232674 http://id.nlm.nih.gov/mesh/M0478431 http://id.nlm.nih.gov/mesh/M0027616 http://id.nlm.nih.gov/mesh/M0023900 http://id.nlm.nih.gov/mesh/M0015042
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Incoming Links

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Total number of triples: 38.