Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders-Reference-Cited by-同舟云学术

Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders

Published:2004-09 Issue:3 Volume:14 Page:131-137
ISSN:0955-8829
Container-title:Psychiatric Genetics
language:en
Short-container-title:Psychiatric Genetics

Author:

Bolton Patrick F.,Veltman Marijcke W. M.,Weisblatt Emma,Holmes Joanne R.,Thomas N. Simon,Youings Sheila A.,Thompson Russell J.,Roberts Siân E.,Dennis Nicholas R.,Browne Caroline E.,Goodson Sally,Moore Vanessa,Brown Josie

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Biological Psychiatry,Psychiatry and Mental health,Genetics(clinical),Genetics

Reference34 articles.

1. Prevalence of the Fragile X Anomaly amongst Autistic Twins and Singletons

2. Genetic studies in autistic disorder and chromosome 15

3. The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders

4. Relationship between clinical and genetic features in “inverted duplicated chromosome 15” patients

5. Inherited Interstitial Duplications of Proximal 15q: Genotype-Phenotype Correlations

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