7282779

Source:http://linkedlifedata.com/resource/pubmed/id/7282779

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0039082, umls-concept:C1317598
pubmed:issue	3
pubmed:dateCreated	1981-11-22
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7708900
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0148-7299
pubmed:author	pubmed-author:CapelozziV LVL, pubmed-author:GonzalezC HCH, pubmed-author:WajntalAA
pubmed:issnType	Print
pubmed:volume	9
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	183-7
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:7282779-Abnormalities, Multiple, pubmed-meshheading:7282779-Chromosome Banding, pubmed-meshheading:7282779-Chromosome Deletion, pubmed-meshheading:7282779-Chromosomes, Human, 4-5, pubmed-meshheading:7282779-Female, pubmed-meshheading:7282779-Humans, pubmed-meshheading:7282779-Infant, Newborn, pubmed-meshheading:7282779-Intellectual Disability, pubmed-meshheading:7282779-Karyotyping, pubmed-meshheading:7282779-Phenotype, pubmed-meshheading:7282779-Syndrome, pubmed-meshheading:7282779-Translocation, Genetic
pubmed:year	1981
pubmed:articleTitle	Pathologic findings in the Wolf-Hirschhorn (4p-) syndrome.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't