Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.
about
Genomic and epigenetic evidence for oxytocin receptor deficiency in autismPartial duplication of the APBA2 gene in chromosome 15q13 corresponds to duplicon structuresGenetics of austim: complex aetiology for a heterogeneous disorderAutism or atypical autism in maternally but not paternally derived proximal 15q duplicationNo evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA networkAutistic symptoms among children and young adults with isodicentric chromosome 15The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)Molecular screening for proximal 15q abnormalities in a mentally retarded population.Three probands with autistic disorder and isodicentric chromosome 15.Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15.Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers.Rearrangements of chromosome 15 in epilepsy.Genetic influences in childhood-onset psychiatric disorders: autism and attention-deficit/hyperactivity disorder.Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.Significant neuronal soma volume deficit in the limbic system in subjects with 15q11.2-q13 duplicationsDifferences between the pattern of developmental abnormalities in autism associated with duplications 15q11.2-q13 and idiopathic autism.Williams Syndrome and 15q Duplication: Coincidence versus Association.A molecular and FISH approach to determining karyotype and phenotype correlations in six patients with supernumerary marker(22) chromosomes.Pervasive developmental disorders and GABAergic system in patients with inverted duplicated chromosome 15.Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder.Autism and maternally derived aberrations of chromosome 15q.Genomic screen and follow-up analysis for autistic disorder.Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.
P2860
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P2860
Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh-hant
name
Cytogenetic and molecular analysis of inv dup
@nl
Cytogenetic and molecular anal ...... sorder and mental retardation.
@en
type
label
Cytogenetic and molecular analysis of inv dup
@nl
Cytogenetic and molecular anal ...... sorder and mental retardation.
@en
prefLabel
Cytogenetic and molecular analysis of inv dup
@nl
Cytogenetic and molecular anal ...... sorder and mental retardation.
@en
P2093
P1476
Cytogenetic and molecular anal ...... sorder and mental retardation.
@en
P2093
Bennett-Baker PE
Flejter WL
Ghaziuddin M
McDonald M
P304
P356
10.1002/(SICI)1096-8628(19960111)61:2<182::AID-AJMG17>3.0.CO;2-Q
P577
1996-01-01T00:00:00Z