reference/16783987

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16783987

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bibliographicCitation	Weh E, Reis LM, Tyler RC, Bick D, Rhead WJ, Wallace S, McGregor TL, Dills SK, Chao M‐, Murray JC, Semina EV. Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes. Clinical Genetics. 2013 Sep 17;86(2):142–8. doi: 10.1111/cge.12241.
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date	2013-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/23889335 https://pubmed.ncbi.nlm.nih.gov/PMC4103962 https://doi.org/10.1111/cge.12241
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes
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