9810860

Source:http://linkedlifedata.com/resource/pubmed/id/9810860

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0016667, umls-concept:C0020202, umls-concept:C0025362, umls-concept:C0392760, umls-concept:C0439660, umls-concept:C1511790, umls-concept:C1521991
pubmed:issue	8-9
pubmed:dateCreated	1998-12-15
pubmed:language	fre
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0413766
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0041-4131
pubmed:author	pubmed-author:AyadiHH, pubmed-author:ChiuY LYL, pubmed-author:FakhfakhFF, pubmed-author:KeskesLL, pubmed-author:MasmoudiSS, pubmed-author:MhiriCC, pubmed-author:TrikiCC, pubmed-author:ViterboBB
pubmed:issnType	Print
pubmed:volume	76
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	244-9
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:9810860-Blotting, Southern, pubmed-meshheading:9810860-Child, pubmed-meshheading:9810860-Diagnosis, Differential, pubmed-meshheading:9810860-Female, pubmed-meshheading:9810860-Fragile X Syndrome, pubmed-meshheading:9810860-Humans, pubmed-meshheading:9810860-In Situ Hybridization, pubmed-meshheading:9810860-Infant, Newborn, pubmed-meshheading:9810860-Intellectual Disability, pubmed-meshheading:9810860-Male, pubmed-meshheading:9810860-Pedigree, pubmed-meshheading:9810860-Pregnancy, pubmed-meshheading:9810860-Prenatal Diagnosis
pubmed:articleTitle	[Detection of fragile X syndrome by molecular hybridization in 29 families affected by hereditary mental retardation].
pubmed:affiliation	Laboratoire d'Immunologie et de Biologie Moléculaire, Faculté de Médecine, Sfax, Tunisie.
pubmed:publicationType	Journal Article