7381872

Source:http://linkedlifedata.com/resource/pubmed/id/7381872

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0035639, umls-concept:C0181586, umls-concept:C1709390
pubmed:issue	2
pubmed:dateCreated	1980-8-15
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/7381872-567620, http://linkedlifedata.com/resource/pubmed/commentcorrection/7381872-700708, http://linkedlifedata.com/resource/pubmed/commentcorrection/7381872-839503
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	0022-2593
pubmed:author	pubmed-author:DezawaTT, pubmed-author:IshiiTT, pubmed-author:KoikeMM, pubmed-author:TsudaNN, pubmed-author:TsukinoRR
pubmed:issnType	Print
pubmed:volume	17
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	148-50
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:7381872-Chromosome Aberrations, pubmed-meshheading:7381872-Chromosome Disorders, pubmed-meshheading:7381872-Chromosomes, Human, 6-12 and X, pubmed-meshheading:7381872-Dermatoglyphics, pubmed-meshheading:7381872-Female, pubmed-meshheading:7381872-Follow-Up Studies, pubmed-meshheading:7381872-Funnel Chest, pubmed-meshheading:7381872-Humans, pubmed-meshheading:7381872-Infant, pubmed-meshheading:7381872-Intellectual Disability, pubmed-meshheading:7381872-Karyotyping, pubmed-meshheading:7381872-Microcephaly, pubmed-meshheading:7381872-Syndrome
pubmed:year	1980
pubmed:articleTitle	Ring chromosome 10:46,XX,r(10)(p15 leads to q26).
pubmed:publicationType	Journal Article, Case Reports