7102724

Source:http://linkedlifedata.com/resource/pubmed/id/7102724

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0796147
pubmed:issue	2
pubmed:dateCreated	1982-9-24
pubmed:abstractText	We report two unrelated patients, a three-year-old girl and an 88/12 year-old boy with the newly described "acrocallosal" syndrome. The main manifestations of the syndrome are unusual facial appearance, pre- and postaxial polydactyly, mental retardation, and absence of the corpus callosum. Cause remains unknown.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7708900
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	0148-7299
pubmed:author	pubmed-author:NelsonM MMM, pubmed-author:ThomsonA JAJ
pubmed:issnType	Print
pubmed:volume	12
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	195-9
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:7102724-Abnormalities, Multiple, pubmed-meshheading:7102724-Agenesis of Corpus Callosum, pubmed-meshheading:7102724-Child, pubmed-meshheading:7102724-Child, Preschool, pubmed-meshheading:7102724-Female, pubmed-meshheading:7102724-Humans, pubmed-meshheading:7102724-Hypertelorism, pubmed-meshheading:7102724-Intellectual Disability, pubmed-meshheading:7102724-Male, pubmed-meshheading:7102724-Orofaciodigital Syndromes, pubmed-meshheading:7102724-Syndrome
pubmed:year	1982
pubmed:articleTitle	The acrocallosal syndrome.
pubmed:publicationType	Journal Article, Case Reports