477407

Source:http://linkedlifedata.com/resource/pubmed/id/477407

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0000772, umls-concept:C0008666, umls-concept:C0008672, umls-concept:C0015671, umls-concept:C0020792, umls-concept:C0026591, umls-concept:C0332597, umls-concept:C0337527, umls-concept:C0441635, umls-concept:C0681850, umls-concept:C0872261, umls-concept:C1550501, umls-concept:C1706203, umls-concept:C2349001, umls-concept:C2349984, umls-concept:C2697811
pubmed:issue	2
pubmed:dateCreated	1979-11-21
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0367735
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0301-0171
pubmed:author	pubmed-author:AronsonM MMM, pubmed-author:BozarthBB, pubmed-author:CoriellL LLL, pubmed-author:GreeneA EAE, pubmed-author:PopeI SIS, pubmed-author:ThulineH CHC
pubmed:issnType	Print
pubmed:volume	24
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	127-8
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:477407-Abnormalities, Multiple, pubmed-meshheading:477407-Child, Preschool, pubmed-meshheading:477407-Chromosome Aberrations, pubmed-meshheading:477407-Chromosome Inversion, pubmed-meshheading:477407-Chromosomes, Human, 1-3, pubmed-meshheading:477407-Chromosomes, Human, 6-12 and X, pubmed-meshheading:477407-Female, pubmed-meshheading:477407-Humans, pubmed-meshheading:477407-Infant, pubmed-meshheading:477407-Male, pubmed-meshheading:477407-XYY Karyotype
pubmed:year	1979
pubmed:articleTitle	Duplication of a segment of chromosome 3 in a subject with multiple congenital anomalies and a 47,XYY father, inversion of chromosomes 3 and 9 in the mother, and inversion of chromosome 9 in a brother. Repository identification Nos. GM-1253, GM-1252, and GM-1251.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Case Reports