reference/9503508

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9503508

Outgoing Links

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contentType	Case Reports\|Journal Article\|Research Support, Non-U.S. Gov't
issn	2324-9269
issueIdentifier	8
pageRange	e774-
publicationName	Molecular Genetics & Genomic Medicine
startingPage	e774
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bibliographicCitation	Souzeau E, Dubowsky A, Ruddle JB, Craig JE. Primary congenital glaucoma due to paternal uniparental isodisomy of chromosome 2 and CYP1B1 deletion. Mol Genet Genomic Med. 2019 Aug;7(8):e774. PMID: 31251480; PMCID: PMC6687653.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_33d581027399d153dc2a5aa344424059 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-2015-6577 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_5323560d76cec7871869579b4202a0aa http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_8d1e685f1582d9caa51d5c37bbe4ce18
date	2019-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/31251480 https://pubmed.ncbi.nlm.nih.gov/PMC6687653 https://doi.org/10.1002/mgg3.774
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/41103 https://portal.issn.org/resource/ISSN/2324-9269
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Primary congenital glaucoma due to paternal uniparental isodisomy of chromosome 2 and CYP1B1 deletion
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Incoming Links

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Total number of triples: 45.