8049905

Source:http://linkedlifedata.com/resource/pubmed/id/8049905

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0004352, umls-concept:C0030551, umls-concept:C0032897, umls-concept:C0332281, umls-concept:C0333715, umls-concept:C0439659
pubmed:issue	1
pubmed:dateCreated	1994-9-8
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9106748
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0955-8829
pubmed:author	pubmed-author:ArrietaII, pubmed-author:CriadoBB, pubmed-author:LobatoM NMN, pubmed-author:MartinezBB
pubmed:issnType	Print
pubmed:volume	4
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	63-5
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:8049905-Autistic Disorder, pubmed-meshheading:8049905-Chromosomes, Human, Pair 15, pubmed-meshheading:8049905-Female, pubmed-meshheading:8049905-Humans, pubmed-meshheading:8049905-Male, pubmed-meshheading:8049905-Prader-Willi Syndrome, pubmed-meshheading:8049905-Translocation, Genetic
pubmed:year	1994
pubmed:articleTitle	Parental origin of Robertsonian translocation (15q22q) and Prader Willi syndrome associated with autism.
pubmed:publicationType	Letter, Case Reports