5114250

Source:http://linkedlifedata.com/resource/pubmed/id/5114250

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008646, umls-concept:C0015780, umls-concept:C0021270, umls-concept:C0039082, umls-concept:C1260969, umls-concept:C1442161
pubmed:issue	9
pubmed:dateCreated	1972-1-5
pubmed:language	pol
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985039R
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	0031-3939
pubmed:author	pubmed-author:BaniowskiAA, pubmed-author:KleczkowskaAA, pubmed-author:Kubie?EE, pubmed-author:SokolowskiJJ
pubmed:issnType	Print
pubmed:volume	46
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1167-70
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:5114250-Abnormalities, Multiple, pubmed-meshheading:5114250-Chromosome Aberrations, pubmed-meshheading:5114250-Chromosome Disorders, pubmed-meshheading:5114250-Chromosomes, Human, 16-18, pubmed-meshheading:5114250-Female, pubmed-meshheading:5114250-Humans, pubmed-meshheading:5114250-Infant, pubmed-meshheading:5114250-Karyotyping
pubmed:year	1971
pubmed:articleTitle	[Syndrome of ring deletion of group E chromosome in a female infant].
pubmed:publicationType	Journal Article