reference/5161873

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/5161873

Outgoing Links

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contentType	Case Reports\|Journal Article\|Research Support, Non-U.S. Gov't
endingPage	60
issn	0340-6717 1432-1203
issueIdentifier	1
pageRange	51-60
publicationName	Human Genetics
startingPage	51
bibliographicCitation	Iseri SU, Wyatt AW, Nürnberg G, Kluck C, Nürnberg P, Holder GE, Blair E, Salt A, Ragge NK. Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy. Hum Genet. 2010 Jul;128(1):51–60. doi: 10.1007/s00439-010-0823-6. PMID: 20414678.
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date	2010-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/20414678 https://doi.org/10.1007/s00439-010-0823-6
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/4137 https://portal.issn.org/resource/ISSN/1432-1203 https://portal.issn.org/resource/ISSN/0340-6717
language	English
source	https://scigraph.springernature.com/ https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy
discusses	http://id.nlm.nih.gov/mesh/M0021788 http://id.nlm.nih.gov/mesh/M0027627 http://id.nlm.nih.gov/mesh/M0470460
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Incoming Links

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Total number of triples: 41.