reference/8803931

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8803931

Outgoing Links

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contentType	Journal Article
endingPage	388
issn	1399-0004 0009-9163
issueIdentifier	3-4
pageRange	386-388
publicationName	Clinical Genetics
startingPage	386
bibliographicCitation	Ricotti R, Nardo T, Striano P, Stefanini M, Orioli D, Botta E. Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal-onset Cockayne syndrome features. Clin Genet. 2018 Oct;94(3-4):386–8. doi: 10.1111/cge.13364. PMID: 29749609.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_4627567319c07aa37c0204fd6ab5669d http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_15a1179b1c589bc35577c38f7eb62f52 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_070a77408e8a897c222a7d7e4a5b6a97 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_2f6325af8de4df96164ad0b9451dbb12 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_cf068a959e8966670f228c474622d046 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0003-2060-0110
date	2018-05-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1111/cge.13364 https://pubmed.ncbi.nlm.nih.gov/29749609
isPartOf	https://portal.issn.org/resource/ISSN/0009-9163 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/3010 https://portal.issn.org/resource/ISSN/1399-0004
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal‐onset Cockayne syndrome features
hasPrimarySubjectTerm	http://id.nlm.nih.gov/mesh/D011296 http://id.nlm.nih.gov/mesh/D003057Q000150 http://id.nlm.nih.gov/mesh/D014983Q000235 http://id.nlm.nih.gov/mesh/D000073537
hasSubjectTerm	http://id.nlm.nih.gov/mesh/D006801 http://id.nlm.nih.gov/mesh/D014983Q000150
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Incoming Links

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Total number of triples: 34.