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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2009-9-8
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pubmed:abstractText |
Results of comparative genomic hybridization studies have suggested that rare copy number variations (CNVs) at numerous loci are involved in the cause of mental retardation, autism spectrum disorders, and schizophrenia.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1538-3636
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pubmed:author |
pubmed-author:AndresChristianC,
pubmed-author:BarthelemyCatherineC,
pubmed-author:BendavidClaudeC,
pubmed-author:Bonnet-BrilhaultFrédériqueF,
pubmed-author:BriaultSylvainS,
pubmed-author:CampionDominiqueD,
pubmed-author:DavidVéroniqueV,
pubmed-author:Di RosaGabriellaG,
pubmed-author:Drouin-GarraudValérieV,
pubmed-author:DubourgChristèleC,
pubmed-author:FaivreLaurenceL,
pubmed-author:FrébourgThierryT,
pubmed-author:GermanoEvaE,
pubmed-author:GoldenbergAliceA,
pubmed-author:GuilmatreAudreyA,
pubmed-author:HenryCélineC,
pubmed-author:ImpallomeniCaterinaC,
pubmed-author:Joly-HelasGéraldineG,
pubmed-author:LaumonnierFrédéricF,
pubmed-author:LayetValérieV,
pubmed-author:Le VaconGaelG,
pubmed-author:LegallicSolennS,
pubmed-author:MoscaAnne-LaureAL,
pubmed-author:OdentSylvieS,
pubmed-author:PinoitJean-MichelJM,
pubmed-author:RosierAntoineA,
pubmed-author:Saugier VeberPascaleP,
pubmed-author:TortorellaGaetanoG
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pubmed:issnType |
Electronic
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pubmed:volume |
66
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
947-56
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:19736351-Adolescent,
pubmed-meshheading:19736351-Adult,
pubmed-meshheading:19736351-Autistic Disorder,
pubmed-meshheading:19736351-Case-Control Studies,
pubmed-meshheading:19736351-Chromosome Mapping,
pubmed-meshheading:19736351-Comparative Genomic Hybridization,
pubmed-meshheading:19736351-Female,
pubmed-meshheading:19736351-Gene Dosage,
pubmed-meshheading:19736351-Gene Frequency,
pubmed-meshheading:19736351-Genotype,
pubmed-meshheading:19736351-Humans,
pubmed-meshheading:19736351-In Situ Hybridization, Fluorescence,
pubmed-meshheading:19736351-Intellectual Disability,
pubmed-meshheading:19736351-Male,
pubmed-meshheading:19736351-Neurogenesis,
pubmed-meshheading:19736351-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:19736351-Proline,
pubmed-meshheading:19736351-Psychotic Disorders,
pubmed-meshheading:19736351-Schizophrenia
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pubmed:year |
2009
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pubmed:articleTitle |
Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation.
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pubmed:affiliation |
Institut National de la Santé et de la Recherche Médicale, Unité 614, Institut Hospitalo-Universitaire de Recherche Biomédicale, 76000 Rouen, France.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Review,
Research Support, Non-U.S. Gov't
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