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Extensive normal copy number variation of a beta-defensin antimicrobial-gene cluster.Association of neuregulin 1 with schizophrenia confirmed in a Scottish populationStructural variation of chromosomes in autism spectrum disorderGenetic and neurodevelopmental influences in autistic disorder.Computing power and sample size for case-control association studies with copy number polymorphism: application of mixture-based likelihood ratio testGenome and gene alterations by insertions and deletions in the evolution of human and chimpanzee chromosome 22.Detection of disease-associated deletions in case-control studies using SNP genotypes with application to rheumatoid arthritis.Disease susceptibility genes for autism.Molecular genetics of autism spectrum disorder.Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism.Strategies for the detection of copy number and other structural variants in the human genome.Whole-genome detection of disease-associated deletions or excess homozygosity in a case-control study of rheumatoid arthritis.De novo balanced translocation t (7;16) (p22.1; p11.2) associated with autistic disorder.The genetic overlap of attention deficit hyperactivity disorder and autistic spectrum disorder.Glutamatergic candidate genes in autism spectrum disorder: an overview.Genome-wide patterns of large-size presence/absence variants in sorghum.Bayesian hierarchical mixture modeling to assign copy number from a targeted CNV array.Exploring the implications of INDELs in neuropsychiatric genetics: challenges and perspectives.The effect of pedigree structure on detection of deletions and other null alleles.A novel partial sequence alignment tool for finding large deletions.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 07 June 2002
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Presence of large deletions in kindreds with autism.
@en
Presence of large deletions in kindreds with autism.
@nl
type
label
Presence of large deletions in kindreds with autism.
@en
Presence of large deletions in kindreds with autism.
@nl
prefLabel
Presence of large deletions in kindreds with autism.
@en
Presence of large deletions in kindreds with autism.
@nl
P2093
P2860
P50
P356
P1476
Presence of large deletions in kindreds with autism.
@en
P2093
Chang-En Yu
Gerard D Schellenberg
Ian D'Souza
Jeffrey Munson
Julie Osterling
M Anne Spence
Moyra Smith
Pamela Flodman
Wendy H Raskind
William McMahon
P2860
P304
P356
10.1086/341291
P407
P577
2002-06-07T00:00:00Z