Duplication of the 15q11-13 Region in a Patient with Autism, Epilepsy and Ataxia-Reference-Cited by-同舟云学术

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Duplication of the 15q11-13 Region in a Patient with Autism, Epilepsy and Ataxia

Published:2008-11-12 Issue:8 Volume:36 Page:736-742
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:

Author:

Bundey Sarah,Hardy Carol,Vickers Susan,Kilpatrick M. W.,Corbett J. A.

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1994.tb11916.x/fullpdf

Reference23 articles.

1. A G-band study of chromosomes in liveborn infants;Buckton;Annals of Human Genetics,1980

2. Cytogenetic survey for autistic fragile X carriers in a mental retardation center;Cantu;American Journal of Mental Retardation,1990

3. A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression;Cattenach;Nature Genetics,1992

4. Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome;Clayton-Smith;Journal of Medical Genetics,1993

5. Duplication in chromosome 15q in a boy with the Prader-Willi syndrome: further cytogenetic confusion;France;Clinical Genetics,1984

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4. Dosage-sensitive genes in autism spectrum disorders: From neurobiology to therapy;Neuroscience & Biobehavioral Reviews;2020-11

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