Source:http://linkedlifedata.com/resource/pubmed/id/15133308
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions |
umls-concept:C0004352,
umls-concept:C0008662,
umls-concept:C0023008,
umls-concept:C0031809,
umls-concept:C0035647,
umls-concept:C0085862,
umls-concept:C0370003,
umls-concept:C0454651,
umls-concept:C1299583,
umls-concept:C1549571,
umls-concept:C1608386,
umls-concept:C1708726,
umls-concept:C1948020,
umls-concept:C2347026
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| pubmed:issue |
1
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| pubmed:dateCreated |
2004-5-10
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| pubmed:abstractText |
Specific language impairment is a neurodevelopmental disorder characterized by impairments essentially restricted to the domain of language and language learning skills. This contrasts with autism, which is a pervasive developmental disorder defined by multiple impairments in language, social reciprocity, narrow interests and/or repetitive behaviors. Genetic linkage studies and family data suggest that the two disorders may have genetic components in common. Two samples, from Canada and the US, selected for specific language impairment were genotyped at loci where such common genes are likely to reside. Significant evidence for linkage was previously observed at chromosome 13q21 in our Canadian sample (HLOD 3.56) and was confirmed in our US sample (HLOD 2.61). Using the posterior probability of linkage (PPL) to combine evidence for linkage across the two samples yielded a PPL over 92%. Two additional loci on chromosome 2 and 7 showed weak evidence for linkage. However, a marker in the cystic fibrosis transmembrane conductance regulator (7q31) showed evidence for association to SLI, confirming results from another group (O'Brien et al. 2003). Our results indicate that using samples selected for components of the autism phenotype may be a useful adjunct to autism genetics.
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| pubmed:grant | |
| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical | |
| pubmed:status |
MEDLINE
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| pubmed:issn |
0001-5652
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| pubmed:author | |
| pubmed:copyrightInfo |
Copyright 2004 S. Karger AG, Basel
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| pubmed:issnType |
Print
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| pubmed:volume |
57
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
10-20
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| pubmed:dateRevised |
2010-12-3
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| pubmed:meshHeading |
pubmed-meshheading:15133308-Autistic Disorder,
pubmed-meshheading:15133308-Canada,
pubmed-meshheading:15133308-Chromosomes, Human, Pair 13,
pubmed-meshheading:15133308-Chromosomes, Human, Pair 2,
pubmed-meshheading:15133308-Chromosomes, Human, Pair 7,
pubmed-meshheading:15133308-Communication Disorders,
pubmed-meshheading:15133308-Cystic Fibrosis Transmembrane Conductance Regulator,
pubmed-meshheading:15133308-Genetic Linkage,
pubmed-meshheading:15133308-Genetic Markers,
pubmed-meshheading:15133308-Genotype,
pubmed-meshheading:15133308-Humans,
pubmed-meshheading:15133308-Language Disorders,
pubmed-meshheading:15133308-Linkage Disequilibrium,
pubmed-meshheading:15133308-Lod Score,
pubmed-meshheading:15133308-Models, Genetic,
pubmed-meshheading:15133308-Phenotype,
pubmed-meshheading:15133308-Statistics as Topic,
pubmed-meshheading:15133308-United States
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| pubmed:year |
2004
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| pubmed:articleTitle |
Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment.
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| pubmed:affiliation |
Center for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA. bartlett@axon.rutgers.edu
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| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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