5313392

Source:http://linkedlifedata.com/resource/pubmed/id/5313392

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008626, umls-concept:C0205210, umls-concept:C0522498, umls-concept:C0868928, umls-concept:C2603343
pubmed:issue	4
pubmed:dateCreated	1971-4-29
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370562
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0003-3995
pubmed:author	pubmed-author:EngelEE, pubmed-author:MooreM KMK
pubmed:issnType	Print
pubmed:volume	13
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	269-74
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:5313392-Abnormalities, Multiple, pubmed-meshheading:5313392-Adolescent, pubmed-meshheading:5313392-Autoradiography, pubmed-meshheading:5313392-Child, pubmed-meshheading:5313392-Chromosome Aberrations, pubmed-meshheading:5313392-Chromosomes, Human, 16-18, pubmed-meshheading:5313392-Chromosomes, Human, 19-20, pubmed-meshheading:5313392-Chromosomes, Human, 21-22 and Y, pubmed-meshheading:5313392-Female, pubmed-meshheading:5313392-Humans, pubmed-meshheading:5313392-Intellectual Disability, pubmed-meshheading:5313392-Karyotyping, pubmed-meshheading:5313392-Mosaicism
pubmed:year	1970
pubmed:articleTitle	Clinical, cytogeneti and autoradiographic studies in 0 cases with rare chromosome disorders. IV. Cases 9 and 10.
pubmed:publicationType	Journal Article