reference/32144491

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/32144491

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endingPage	45
issn	1552-4825 1552-4833
issueIdentifier	1
pageRange	39-45
publicationName	American journal of medical genetics. Part A
startingPage	39
bibliographicCitation	Faiyaz‐Ul‐Haque M, Zaidi SHE, Al‐Ali M, Al‐Mureikhi MS, Kennedy S, Al‐Thani G, Tsui L, Teebi AS. A novel missense mutation in the galactosyltransferase‐I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers–Danlos syndrome resembling the progeroid type. American J of Med Genetics Pt A. 2004 Mar 23;128A(1):39–45. doi: 10.1002/ajmg.a.30005.
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date	2004-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/15211654 https://doi.org/10.1002/ajmg.a.30005
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	A novel missense mutation in the galactosyltransferase‐I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers–Danlos syndrome resembling the progeroid type
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Total number of triples: 57.