A “new” chromosome marker common to the Rett syndrome and infantile autism? the frequency of fragile sites at X P22 in 81 children with infantile autism, childhood psychosis and the Rett syndrome-Reference-Cited by-同舟云学术

A “new” chromosome marker common to the Rett syndrome and infantile autism? the frequency of fragile sites at X P22 in 81 children with infantile autism, childhood psychosis and the Rett syndrome

Published:1985-01 Issue:3 Volume:7 Page:365-367
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Gillberg Christopher,Wahlström Jan,Hagberg Bengt

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference12 articles.

1. Early infantile autism: 1943–1955;Kanner;Am J Orthopsychiatry,1956

2. The Biology of the Autistic Syndromes;Coleman,1985

3. Diagnostic and statistical manual of mental disorders,1980

4. Diagnosis and definition;Rutter,1978

5. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett syndrome: report of 35 cases;Hagberg;Ann Neurol,1983

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1. Fragile sites, chromosomal lesions, tandem repeats, and disease;Frontiers in Genetics;2022-11-17

2. Dolor en personas adultas con un trastorno del espectro del autismo (TEA) y comorbilidad: un análisis mediacional;REVISTA ESPAÑOLA DE DISCAPACIDAD;2017-12-26

3. The Syndromes Described by Kanner and Rett-Hagberg: Overlap in an Extended Family;Developmental Medicine & Child Neurology;2010-08-24

4. Report on the Rett Syndrome Workshop: Glasgow, Scotland, 24-25 May 1986;Journal of Intellectual Disability Research;2008-06-28

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