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PMID: 7961335 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, P.H.S.

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

Journal of autism and developmental disorders ·Vol. 24 ·No. 4 ·1994-08-00 ·Pages 529-35

Baker P, Piven J, Schwartz S, Patil S

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/genetics,psychology Autistic Disorder/genetics,psychology Child Chromosome Aberrations/genetics Chromosome Banding Chromosome Disorders Chromosome Mapping Chromosomes, Human, Pair 15 Female Humans Intellectual Disability/genetics,psychology Language Development Disorders/genetics,psychology

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Baker P

Department of Psychiatry, University of Iowa College of Medicine.

Piven J

Schwartz S

Patil S

References (10)

10 references, click to expand

Clinical and molecular analysis of five inv dup(15) patients.
Eur J Hum Genet. 1993;1(1):37-50 PMID: 8069650
Autism associated with marker chromosome.
J Am Acad Child Adolesc Psychiatry. 1991 May;30(3):489-94 PMID: 2055888
Cytogenetic and clinical studies in five cases of inv dup(15).
Hum Genet. 1979 Sep;50(3):259-70 PMID: 489010
Etiology of autism: genetic influences.
Pediatrics. 1991 May;87(5 Pt 2):767-73 PMID: 1708492
Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A.
Nat Genet. 1992 Apr;1(1):29-33 PMID: 1301995
The prevalence of fragile X in a sample of autistic individuals diagnosed using a standardized interview.
J Am Acad Child Adolesc Psychiatry. 1991 Sep;30(5):825-30 PMID: 1938801
Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases.
Am J Hum Genet. 1982 Mar;34(2):278-85 PMID: 7072717
Why are autism and the fragile-X syndrome associated? Conceptual and methodological issues.
Am J Hum Genet. 1991 Feb;48(2):195-202 PMID: 1990832
Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15.
Am J Hum Genet. 1991 Aug;49(2):330-7 PMID: 1714232
Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.
N Engl J Med. 1981 Feb 5;304(6):325-9 PMID: 7442771

Article Info

Journal

Journal of autism and developmental disorders

Abbr.

J Autism Dev Disord

ISSN

0162-3257

DOI

10.1007/BF02172133

Published

1994-08-00

Pages

529-35

Language

English

Region

United States

NLM ID

7904301

Subset

Grants

NIMH NIH HHS · NIMH MH-01028-02 · United States

External Links

PubMed source DOI: 10.1007/BF02172133 View journal details

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

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