Parental origin of Robertsonian translocation (15q22q) and Prader Willi syndrome associated with autism-Reference-Cited by-同舟云学术

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Parental origin of Robertsonian translocation (15q22q) and Prader Willi syndrome associated with autism

Published:1994 Issue:1 Volume:4 Page:63-66
ISSN:0955-8829
Container-title:Psychiatric Genetics
language:en
Short-container-title:Psychiatric Genetics

Author:

Arrieta I.,Lobato M. N.,Martinez B.,Criado B.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

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

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinicopathological Stratification of Idiopathic Autism and Autism with 15q11.2–q13 Duplications;The Neuroscience of Autism Spectrum Disorders;2013

2. Association of GABRB3 Polymorphisms with Autism Spectrum Disorders in Korean Trios;Neuropsychobiology;2006

3. Autism spectrum disorders in Prader???Willi and Angelman syndromes: a systematic review;Psychiatric Genetics;2005-12

4. Fine Mapping of Autistic Disorder to Chromosome 15q11-q13 by Use of Phenotypic Subtypes;The American Journal of Human Genetics;2003-03

5. Genomic screen and follow-up analysis for autistic disorder;American Journal of Medical Genetics;2002-01-08

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