reference/27574455

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/27574455

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publicationName	American journal of medical genetics. Part A
startingPage	2574
bibliographicCitation	Hogue J, Shankar S, Perry H, Patel R, Vargervik K, Slavotinek A. A novel EFNB1 mutation (c.712delG) in a family with craniofrontonasal syndrome and diaphragmatic hernia. American J of Med Genetics Pt A. 2010 Aug 23;152A(10):2574–7. doi: 10.1002/ajmg.a.33596.
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date	2010-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/ajmg.a.33596 https://pubmed.ncbi.nlm.nih.gov/20734337
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	A novel EFNB1 mutation (c.712delG) in a family with craniofrontonasal syndrome and diaphragmatic hernia
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Total number of triples: 49.