Literature DB >> 8334323

Abnormalities of chromosome 18 in a girl with mental retardation and autistic disorder.

M Ghaziuddin1, S Sheldon, L Y Tsai, N Alessi.   

Abstract

Structural autosome defects have rarely been described in autism. In this report, the authors describe the association of autism and mental retardation in a girl with mosaicism for a duplication of the long arm of chromosome 18 and a deletion of the short arm of chromosome 18.

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Year:  1993        PMID: 8334323     DOI: 10.1111/j.1365-2788.1993.tb01288.x

Source DB:  PubMed          Journal:  J Intellect Disabil Res        ISSN: 0964-2633


  5 in total

1.  Maternal origin of inv dup(15) chromosomes in infantile autism.

Authors:  T Martinsson; T Johannesson; M Vujic; A Sjöstedt; S Steffenburg; C Gillberg; J Wahlström
Journal:  Eur Child Adolesc Psychiatry       Date:  1996-12       Impact factor: 4.785

2.  Elective mutism and chromosome 18 abnormality.

Authors:  D Simons; S Goode; E Fombonne
Journal:  Eur Child Adolesc Psychiatry       Date:  1997-06       Impact factor: 4.785

3.  Chromosomal abnormalities in a series of children with autistic disorder.

Authors:  M M Konstantareas; S Homatidis
Journal:  J Autism Dev Disord       Date:  1999-08

4.  Somatic genome variations in health and disease.

Authors:  I Y Iourov; S G Vorsanova; Y B Yurov
Journal:  Curr Genomics       Date:  2010-09       Impact factor: 2.236

5.  Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder.

Authors:  Kavita S Reddy
Journal:  BMC Med Genet       Date:  2005-01-18       Impact factor: 2.103

  5 in total

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