3703649

Source:http://linkedlifedata.com/resource/pubmed/id/3703649

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0243095, umls-concept:C0332281, umls-concept:C0795799, umls-concept:C1299003, umls-concept:C2700116
pubmed:issue	5
pubmed:dateCreated	1986-6-2
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0376422
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0031-4005
pubmed:author	pubmed-author:KareshJJ, pubmed-author:SchwartzM FMF, pubmed-author:SchwartzSS, pubmed-author:WrightL LLL
pubmed:issnType	Print
pubmed:volume	77
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	786
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:3703649-Abnormalities, Multiple, pubmed-meshheading:3703649-Chromosome Aberrations, pubmed-meshheading:3703649-Chromosome Deletion, pubmed-meshheading:3703649-Chromosome Disorders, pubmed-meshheading:3703649-Chromosomes, Human, 1-3, pubmed-meshheading:3703649-Female, pubmed-meshheading:3703649-Humans, pubmed-meshheading:3703649-Infant, Newborn
pubmed:year	1986
pubmed:articleTitle	An unusual ocular finding associated with chromosome 1q deletion syndrome.
pubmed:publicationType	Letter, Case Reports