15342694

Source:http://linkedlifedata.com/resource/pubmed/id/15342694

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:C0012655, umls-concept:C0013331, umls-concept:C0015576, umls-concept:C0034606, umls-concept:C0231449, umls-concept:C0441633, umls-concept:C0476254, umls-concept:C1708726, umls-concept:C1710698
pubmed:issue	9
pubmed:dateCreated	2004-9-2
pubmed:abstractText	Dyslexia is a common disorder with a strong genetic component, but despite significant research effort, the aetiology is still largely unknown.
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-10100857, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-10507721, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-10677331, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-10749993, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-10924405, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-11454705, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-11584043, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-11743577, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-11806692, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-11836362, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-12076671, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-12360321, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-12642493, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-12746395, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-12954984, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-15503588, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-1612212, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-1880884, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-3344216, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-3957003, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-6585139, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-7939663, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-8101276, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-8651263, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-8981944, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-9345087, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-9634505, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-9634517, http://linkedlifedata.com/resource/pubmed/commentcorrection/15342694-9881668
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	1468-6244
pubmed:author	pubmed-author:FrankeBB, pubmed-author:HeisterJ G A MJG, pubmed-author:PadbergG WGW, pubmed-author:SandkuijlL ALA, pubmed-author:SheY YYY, pubmed-author:WillemenJ J H TJJ, pubmed-author:de KovelC G FCG
pubmed:issnType	Electronic
pubmed:volume	41
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	652-7
pubmed:dateRevised	2009-11-18
pubmed:meshHeading	pubmed-meshheading:15342694-Adolescent, pubmed-meshheading:15342694-Adult, pubmed-meshheading:15342694-Aged, pubmed-meshheading:15342694-Alleles, pubmed-meshheading:15342694-Chromosomes, Human, X, pubmed-meshheading:15342694-DNA Mutational Analysis, pubmed-meshheading:15342694-Dyslexia, pubmed-meshheading:15342694-Female, pubmed-meshheading:15342694-Genes, Dominant, pubmed-meshheading:15342694-Genetic Diseases, X-Linked, pubmed-meshheading:15342694-Genetic Predisposition to Disease, pubmed-meshheading:15342694-Genome, Human, pubmed-meshheading:15342694-Humans, pubmed-meshheading:15342694-Lod Score, pubmed-meshheading:15342694-Male, pubmed-meshheading:15342694-Middle Aged, pubmed-meshheading:15342694-Netherlands, pubmed-meshheading:15342694-Pedigree, pubmed-meshheading:15342694-Quantitative Trait Loci, pubmed-meshheading:15342694-Questionnaires, pubmed-meshheading:15342694-Reading, pubmed-meshheading:15342694-Sex Characteristics, pubmed-meshheading:15342694-Siblings
pubmed:year	2004
pubmed:articleTitle	Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.
pubmed:affiliation	Department of Theoretical Biology, University of Leiden, NL-2311 GP Leiden, The Netherlands. dekovel@rulsfb.leidenuniv.ne
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't