(Q50301513)

2 March 2018

review article

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title

Chromosomal disorders and autism (English)

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2 March 2018

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C Gillberg

1

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2 March 2018

language of work or name

English

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publication date

1 October 1998

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2 March 2018

Journal of Autism and Developmental Disorders

published in

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2 March 2018

volume

28

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2 March 2018

issue

5

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2 March 2018

page(s)

415-425

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2 March 2018

Behavior checklist for identifying severely handicapped individuals with high levels of autistic behavior.

cites work

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Partial 6p trisomy associated with infantile autism

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The early development of autistic children

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Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases

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Infantile autism and Rett's syndrome: common chromosomal denominator

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Serum serotonin, free tryptophan and plasma cyclic AMP levels in autistic children -with special reference to their relation to hyperkinesia

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Obesity and abnormal behaviour associated with interstitial deletion of chromosome 18 (q12.2q21.1).

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Toward objective classification of childhood autism: Childhood Autism Rating Scale (CARS)

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Autism, mental retardation, multiple exostoses and short stature in a female with 46,X,t(X;8)(p22.13;q22.1).

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Clinical consequences of deletion 1p35.

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Effects of the XYY karyotype in one of two brothers with congenital adrenal hyperplasia

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Partial trisomy 16p in an adolescent with autistic disorder and Tourette's syndrome

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Neuropsychiatry of 18q- syndrome

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Fragile X syndrome in autistic boys

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Asperger syndrome in a boy with a balanced de novo translocation: t(17;19)(p13.3;p11)

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Chromosome subband 17p11.2 deletion: a minute deletion syndrome.

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Autism and ring chromosome 18 mosaicism

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Idiopathic thrombocytopenic purpura with X chromosome abnormality

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

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Fra(2) (q13) and inv(9) (p11q12) in autism: causal relationship?

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Childhood of males with the XYY syndrome

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Hypomelanosis of Ito in Three Cases with Autism and Autistic-like Conditions

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Autistic disorder and additional inv dup(15)(pter----q13) chromosome

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Autism: the point of view from fragile X studies

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Childhood Psychosis Combined with XYY Abnormalities

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Brief report: autism of the Asperger type associated with an autosomal fragile site

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A genetic-diagnostic survey in an institutionalized population of 173 severely mentally retarded patients

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A clinical and molecular study of mosaicism for trisomy 17.

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Chromosomal abnormalities in a psychiatric population

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Mapping of the human adenylosuccinate lyase (ADSL) gene to chromosome 22q13.1-->q13.2.

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Autism, mental retardation, and chromosomal abnormalities

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Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia.

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Marker chromosome 21 identified by microdissection and FISH.

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Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).

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Twins with autism and mental retardation associated with balanced (7;20) chromosomal translocation

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Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder

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The morbid anatomy of the human genome: chromosomal location of mutations causing disease

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A complex chromosome rearrangement in a boy with autism.

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Electroretinograms in autism: a pilot study of b-wave amplitudes

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Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesis

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12 December 2020

Neurobiological findings in 20 relatively gifted children with Kanner-type autism or Asperger syndrome

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Distal deletion of chromosome 1q in an adult

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12 December 2020

Autism, profound mental retardation and atypical bipolar disorder in a 33-year-old female with a deletion of 15q12.

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12 December 2020

Infantile autism among children in the county of Nordland. Prevalence and etiology

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12 December 2020

Molecular cytogenetic analysis of a duplication Xp in a male: further delineation of a possible sex influencing region on the X chromosome.

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12 December 2020

18q- chromosomal abnormality in a phenotypically normal 2 1/2-year-old male with autism

1 reference

12 December 2020

A case of autism associated with partial tetrasomy 15

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1026004505764

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2 March 2018

Dimensions Publication ID

1027186553

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2 March 2018