18582721

Source:http://linkedlifedata.com/resource/pubmed/id/18582721

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:C0025362
pubmed:issue	5
pubmed:dateCreated	2008-6-27
pubmed:language	fre
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9421356
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	0929-693X
pubmed:author	pubmed-author:JournelHH, pubmed-author:LazaroLL, pubmed-author:OdentSS, pubmed-author:PasquierLL, pubmed-author:de la RochebrochardCC
pubmed:issnType	Print
pubmed:volume	15
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	705-7
pubmed:meshHeading	pubmed-meshheading:18582721-Child, pubmed-meshheading:18582721-Chromosome Aberrations, pubmed-meshheading:18582721-Humans, pubmed-meshheading:18582721-Mental Disorders, pubmed-meshheading:18582721-Syndrome
pubmed:year	2008
pubmed:articleTitle	[Syndromic mental retardation].
pubmed:affiliation	Service de génétique clinique, CHU de Rennes Hôpital Sud, 16 Bd de Bulgarie, BP 90 347, 35 203 Rennes cedex 2. sylvie.odent@chu-rennes.fr <sylvie.odent@chu-rennes.fr>
pubmed:publicationType	Journal Article