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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2009-4-9
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pubmed:abstractText |
Segmental duplications at breakpoints (BP4-BP5) of chromosome 15q13.2q13.3 mediate a recurrent genomic imbalance syndrome associated with mental retardation, epilepsy, and/or electroencephalogram (EEG) abnormalities.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1468-6244
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pubmed:author |
pubmed-author:AnselmII,
pubmed-author:BridgemohanCC,
pubmed-author:DickinsonHH,
pubmed-author:GaleA MAM,
pubmed-author:GentileJJ,
pubmed-author:GusellaJ FJF,
pubmed-author:HarrisD JDJ,
pubmed-author:HegdeVV,
pubmed-author:HundleyRR,
pubmed-author:KhwajaOO,
pubmed-author:KornJJ,
pubmed-author:KothareSS,
pubmed-author:LuedkeCC,
pubmed-author:MillerD TDT,
pubmed-author:MokM MMM,
pubmed-author:NasirRR,
pubmed-author:PoduriAA,
pubmed-author:PrasadKK,
pubmed-author:RAOS NSN,
pubmed-author:RaffalliPP,
pubmed-author:ReinhardAA,
pubmed-author:SelfP RPR,
pubmed-author:ShenYY,
pubmed-author:SmithS ESE,
pubmed-author:SobeihM MMM,
pubmed-author:StolerJJ,
pubmed-author:TakeokaMM,
pubmed-author:ThakuriaJJ,
pubmed-author:WeissL ALA,
pubmed-author:WolffRR,
pubmed-author:WuB-LBL,
pubmed-author:YusupovRR
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pubmed:issnType |
Electronic
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pubmed:volume |
46
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
242-8
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:18805830-Adolescent,
pubmed-meshheading:18805830-Autistic Disorder,
pubmed-meshheading:18805830-Child,
pubmed-meshheading:18805830-Child, Preschool,
pubmed-meshheading:18805830-Chromosome Aberrations,
pubmed-meshheading:18805830-Chromosome Deletion,
pubmed-meshheading:18805830-Chromosomes, Human, Pair 15,
pubmed-meshheading:18805830-Comparative Genomic Hybridization,
pubmed-meshheading:18805830-Female,
pubmed-meshheading:18805830-Gene Duplication,
pubmed-meshheading:18805830-Humans,
pubmed-meshheading:18805830-Infant,
pubmed-meshheading:18805830-Intellectual Disability,
pubmed-meshheading:18805830-Male,
pubmed-meshheading:18805830-Phenotype,
pubmed-meshheading:18805830-Young Adult
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pubmed:year |
2009
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pubmed:articleTitle |
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
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pubmed:affiliation |
Department of Laboratory Medicine, Children's Hospital Boston, 300 Longwood Ave, Boston, Massachusetts 02115, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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