reference/25985813

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/25985813

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	2150
issn	0964-6906 1460-2083
issueIdentifier	11
pageRange	2145-2150
publicationName	Human Molecular Genetics
startingPage	2145
bibliographicCitation	Kok YJMD, Merkx GFM, van der Maarel SM, Huber I, Malcolm S, Ropers H-, Cremers FPM. A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene. Human Molecular Genetics. 1995 Nov 01;4(11):2145–50. doi: 10.1093/hmg/4.11.2145.
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date	1995-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/8589693 https://doi.org/10.1093/hmg/4.11.2145
isPartOf	https://portal.issn.org/resource/ISSN/0964-6906 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/2407 https://portal.issn.org/resource/ISSN/1460-2083
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene
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Total number of triples: 49.