reference/15410104

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/15410104

Outgoing Links

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endingPage	184
issn	1552-4868 1552-4876
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pageRange	178-184
publicationName	American journal of medical genetics. Part C, Seminars in medical genetics
startingPage	178
bibliographicCitation	Vermeer AM, van Engelen K, Postma AV, Baars MJ, Christiaans I, De Haij S, Klaassen S, Mulder BJ, Keavney B. Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7. Am J Med Genet C Semin Med Genet. 2013 Aug;163C(3):178–84. doi: 10.1002/ajmg.c.31365. PMID: 23794396.
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date	2013-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/ajmg.c.31365 https://pubmed.ncbi.nlm.nih.gov/23794396
isPartOf	https://portal.issn.org/resource/ISSN/1552-4868 https://portal.issn.org/resource/ISSN/1552-4876 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/32213
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Ebstein anomaly associated with left ventricular noncompaction: An autosomal dominant condition that can be caused by mutations in MYH7
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Total number of triples: 51.