reference/26816212

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/26816212

Outgoing Links

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endingPage	122
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pageRange	114-122
publicationName	Journal of Cellular Physiology
startingPage	114
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bibliographicCitation	Kim HJ, Nam SH, Kim HJ, Park HS, Ryoo HM, Kim SY, Cho TJ, Kim SG, Bae SC, Kim IS, Stein JL, van Wijnen AJ, Stein GS, Lian JB, Choi JY. Four novel RUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype. J Cell Physiol. 2006 Apr;207(1):114–22. doi: 10.1002/jcp.20552. PMID: 16270353.
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date	2005-11-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Four novel RUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype
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