reference/8686893

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8686893

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	258
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publicationName	The American Journal of Human Genetics
startingPage	252
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bibliographicCitation	Moffatt P, Ben Amor M, Glorieux FH, Roschger P, Klaushofer K, Schwartzentruber JA, Paterson AD, Hu P, Marshall C; FORGE Canada Consortium, Fahiminiya S, Majewski J, Beaulieu CL, Boycott KM, Rauch F. Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly is caused by a duplication in RUNX2. Am J Hum Genet. 2013 Feb 07;92(2):252–8. PMID: 23290074; PMCID: PMC3567275.
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date	2013-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1016/j.ajhg.2012.12.001 https://pubmed.ncbi.nlm.nih.gov/PMC3567275 https://pubmed.ncbi.nlm.nih.gov/23290074
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly Is Caused by a Duplication in RUNX2
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