5588739

Source:http://linkedlifedata.com/resource/pubmed/id/5588739

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0040715, umls-concept:C0241888, umls-concept:C0599718, umls-concept:C0599813, umls-concept:C0599893, umls-concept:C1522702
pubmed:issue	2
pubmed:dateCreated	1968-8-6
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7507223
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0037-5683
pubmed:author	pubmed-author:BoonW HWH
pubmed:issnType	Print
pubmed:volume	9
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	88-93
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:5588739-Asian Continental Ancestry Group, pubmed-meshheading:5588739-Chromosome Aberrations, pubmed-meshheading:5588739-Chromosome Disorders, pubmed-meshheading:5588739-Female, pubmed-meshheading:5588739-Humans, pubmed-meshheading:5588739-Infant, Newborn, pubmed-meshheading:5588739-Karyotyping
pubmed:year	1967
pubmed:articleTitle	Familial 2/3 translocation.
pubmed:publicationType	Journal Article, Case Reports