10802779

Source:http://linkedlifedata.com/resource/pubmed/id/10802779

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:C0031437, umls-concept:C0039593, umls-concept:C0162791, umls-concept:C0348026, umls-concept:C1540039, umls-concept:C1851945
pubmed:issue	9
pubmed:dateCreated	2000-5-30
pubmed:abstractText	To develop diagnostic testing guidelines for the DYT1 GAG deletion in the Ashkenazi Jewish (AJ) and non-Jewish (NJ) primary torsion dystonia (PTD) populations and to determine the range of dystonic features in affected DYT1 deletion carriers.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/NS26656, http://linkedlifedata.com/resource/pubmed/grant/NS28384
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/10802779-10802773
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Molecular Chaperones, http://linkedlifedata.com/resource/pubmed/chemical/TOR1A protein, human
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0028-3878
pubmed:author	pubmed-author:BreakefieldXX, pubmed-author:BressmanS BSB, pubmed-author:BrinM FMF, pubmed-author:FahnSS, pubmed-author:KleinCC, pubmed-author:KramerP LPL, pubmed-author:OzeliusL JLJ, pubmed-author:RaymondDD, pubmed-author:RischN JNJ, pubmed-author:SabattiCC, pubmed-author:de LeonDD
pubmed:issnType	Print
pubmed:day	9
pubmed:volume	54
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1746-52
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:10802779-Adolescent, pubmed-meshheading:10802779-Adult, pubmed-meshheading:10802779-Aged, pubmed-meshheading:10802779-Carrier Proteins, pubmed-meshheading:10802779-Child, pubmed-meshheading:10802779-Child, Preschool, pubmed-meshheading:10802779-Chromosome Deletion, pubmed-meshheading:10802779-Dystonia Musculorum Deformans, pubmed-meshheading:10802779-Female, pubmed-meshheading:10802779-Genetic Counseling, pubmed-meshheading:10802779-Genetic Testing, pubmed-meshheading:10802779-Heterozygote Detection, pubmed-meshheading:10802779-Humans, pubmed-meshheading:10802779-Jews, pubmed-meshheading:10802779-Male, pubmed-meshheading:10802779-Middle Aged, pubmed-meshheading:10802779-Molecular Chaperones, pubmed-meshheading:10802779-Phenotype, pubmed-meshheading:10802779-Polymerase Chain Reaction, pubmed-meshheading:10802779-Practice Guidelines as Topic, pubmed-meshheading:10802779-Predictive Value of Tests
pubmed:year	2000
pubmed:articleTitle	The DYT1 phenotype and guidelines for diagnostic testing.
pubmed:affiliation	Department of Neurology, Beth Israel Medical Center, New York, NY 10003, USA.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't