reference/3935945

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3935945

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publicationName	American journal of medical genetics. Part A
startingPage	2489
bibliographicCitation	Ovaert C, Busa T, Faure E, Missirian C, Philip N, Paoli F, Milh M, Macé L, Zaffran S. FOXC1 haploinsufficiency due to 6p25 deletion in a patient with rapidly progressing aortic valve disease. American J of Med Genetics Pt A. 2017 Jun 28;173(9):2489–93. doi: 10.1002/ajmg.a.38331.
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date	2017-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/ajmg.a.38331 https://pubmed.ncbi.nlm.nih.gov/28657660
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	FOXC1 haploinsufficiency due to 6p25 deletion in a patient with rapidly progressing aortic valve disease
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