18q- Chromosomal Abnormality in a Phenotypically Normal 21/2-year-Old Male with Autism-Reference-Cited by-同舟云学术

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18q- Chromosomal Abnormality in a Phenotypically Normal 21/2-year-Old Male with Autism

Published:2008-11-12 Issue:11 Volume:34 Page:1005-1009
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:

Author:

Seshadri Kapila,Wallerstein Robert,Burack Gail,Johnson Robert Wood

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1992.tb11406.x/fullpdf

Reference17 articles.

1. Childhood psychosis combined with XYY abnormalities;Abrams;Journal of Genetic Psychology,1971

2. Hypomelanosis of Ito in three cases with autism and autistic-like conditions;Åkefeldt;Developmental Medicine and Child Neurology,1991

3. Autistic disorder associated with an iso-dicentric Y chromosome;Blackman;Developmental Medicine and Child Neurology,1991

4. Hypoplasia of cerebellar vermal lobules VI and VII in autism;Courchesne;New England Journal of Medicine,1988

Cited by 3 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. Development, cognition, and behaviour in Pitt-Hopkins syndrome;Developmental Medicine & Child Neurology;2012-06-19

2. BIBLIOGRAPHY OF DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY: SELECTED BOOKS AND ARTICLES RECEIVED IN 1992;Developmental Medicine & Child Neurology;2008-11-12

3. Cytogenetic abnormalities and fragile-x syndrome in Autism Spectrum Disorder;BMC Medical Genetics;2005-01-18

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