8571973

Source:http://linkedlifedata.com/resource/pubmed/id/8571973

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0012634, umls-concept:C0035298, umls-concept:C0439660, umls-concept:C0600281
pubmed:issue	2
pubmed:dateCreated	1996-3-1
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/8571973-1138842, http://linkedlifedata.com/resource/pubmed/commentcorrection/8571973-5764685, http://linkedlifedata.com/resource/pubmed/commentcorrection/8571973-7611300
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370475
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	0002-9297
pubmed:author	pubmed-author:HardcastleA JAJ, pubmed-author:InglehearnC FCF
pubmed:issnType	Print
pubmed:volume	58
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	433-5
pubmed:dateRevised	2009-11-18
pubmed:meshHeading	pubmed-meshheading:8571973-Chromosome Mapping, pubmed-meshheading:8571973-Female, pubmed-meshheading:8571973-Genes, Dominant, pubmed-meshheading:8571973-Genes, Recessive, pubmed-meshheading:8571973-Humans, pubmed-meshheading:8571973-Male, pubmed-meshheading:8571973-Phenotype, pubmed-meshheading:8571973-Retinal Degeneration, pubmed-meshheading:8571973-Retinitis Pigmentosa, pubmed-meshheading:8571973-Terminology as Topic, pubmed-meshheading:8571973-X Chromosome
pubmed:year	1996
pubmed:articleTitle	Nomenclature for inherited diseases of the retina.
pubmed:publicationType	Letter, Comment