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Molecular genetic investigations of autism.

作者信息

Maestrini E, Marlow A J, Weeks D E, Monaco A P

机构信息

Wellcome Trust Centre for Human Genetics, Oxford, United Kingdom.

出版信息

J Autism Dev Disord. 1998 Oct;28(5):427-37. doi: 10.1023/a:1026056522602.

DOI:10.1023/a:1026056522602
PMID:9813778
Abstract

Genetic factors are likely to play a major role in the etiology of autism. The genetics of the disorder is however complex, probably involving the action of several genes. In an attempt to identify autism susceptibility loci we are currently undertaking a systematic screening of the whole human genome using multiplex families. We describe the resources and the methods needed to achieve such a task, including extensive collection of family data, semiautomated genotyping technology, and specialized statistical approaches for linkage analysis of complex traits.

摘要

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引用本文的文献

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Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.利用表型亚型将孤独症谱系障碍精细定位到15号染色体q11-q13区域。
Am J Hum Genet. 2003 Mar;72(3):539-48. doi: 10.1086/367846. Epub 2003 Feb 3.

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Autism and the X chromosome. Multipoint sib-pair analysis.自闭症与X染色体。多点同胞对分析。
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10
A gene map of the human genome.人类基因组的基因图谱。
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