2715785

Source:http://linkedlifedata.com/resource/pubmed/id/2715785

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0032897, umls-concept:C0205210, umls-concept:C0205460, umls-concept:C0868928, umls-concept:C2603343
pubmed:issue	1
pubmed:dateCreated	1989-6-14
pubmed:abstractText	Clinical and cytogenetic studies are performed on 14 patients with PWS including endocrinological investigations, as coagulation factor XI activity and pigmentation studies. Recent hypothesis from molecular analysis are discussed.
pubmed:language	fre
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2983308R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Factor XI
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	0021-7743
pubmed:author	pubmed-author:GilgenkrantzSS, pubmed-author:KarpJ CJC, pubmed-author:LeheupBB, pubmed-author:MujicaPP, pubmed-author:PiersonMM
pubmed:issnType	Print
pubmed:volume	37
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	77-86
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:2715785-Abnormalities, Multiple, pubmed-meshheading:2715785-Chromosome Aberrations, pubmed-meshheading:2715785-Chromosome Banding, pubmed-meshheading:2715785-Chromosome Disorders, pubmed-meshheading:2715785-Chromosomes, Human, Pair 15, pubmed-meshheading:2715785-Factor XI, pubmed-meshheading:2715785-Growth Disorders, pubmed-meshheading:2715785-Humans, pubmed-meshheading:2715785-Obesity, pubmed-meshheading:2715785-Phenotype, pubmed-meshheading:2715785-Pigmentation Disorders, pubmed-meshheading:2715785-Syndrome
pubmed:year	1989
pubmed:articleTitle	[Clinical and biological studies of 14 cases of the Prader-Labhart-Willi syndrome].
pubmed:affiliation	Laboratoire de Génétique, C.R.T.S., Nancy.
pubmed:publicationType	Journal Article, English Abstract