reference/398134

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/398134

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	E1593
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publicationName	Human Mutation
startingPage	E1587
bibliographicCitation	Ott CE, Leschik G, Trotier F, Brueton L, Brunner HG, Brussel W, Guillen-Navarro E, Haase C, Kohlhase J, Kotzot D, Lane A, Lee-Kirsch MA, Morlot S, Simon ME, Steichen-Gersdorf E, Tegay DH, Peters H, Mundlos S, Klopocki E. Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia. Hum Mutat. 2010 Aug;31(8):E1587–93. doi: 10.1002/humu.21298. PMID: 20648631.
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date	2010-06-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/20648631 https://doi.org/10.1002/humu.21298
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia
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Incoming Links

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Total number of triples: 52.