Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.
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Genetics evaluation for the etiologic diagnosis of autism spectrum disordersGenetics of autism spectrum disorderMultiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.Molecular cytogenetics and cytogenomics of brain diseases.Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism.De novo balanced translocation t (7;16) (p22.1; p11.2) associated with autistic disorder.Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13.1p13.3 and 10q26.3 Duplications.Unexplained autism is frequently associated with low-level mosaic aneuploidy.Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area.Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism.
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P2860
Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.
description
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name
Chromosomal anomalies in indiv ...... n of genes involved in autism.
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Chromosomal anomalies in indiv ...... n of genes involved in autism.
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type
label
Chromosomal anomalies in indiv ...... n of genes involved in autism.
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Chromosomal anomalies in indiv ...... n of genes involved in autism.
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Chromosomal anomalies in indiv ...... n of genes involved in autism.
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Chromosomal anomalies in indiv ...... n of genes involved in autism.
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Chromosomal anomalies in indiv ...... on of genes involved in autism
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Dries Castermans
Jean-Pierre Fryns
Koen Devriendt
Valérie Wilquet
Wim Van de Ven
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P304
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10.1177/1362361304042719
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2004-06-01T00:00:00Z