Different approaches to relating genotype to phenotype in developmental disorders

被引:44
作者
Karmiloff-Smith, A [1 ]
Scerif, G [1 ]
Thomas, M [1 ]
机构
[1] Inst Child Hlth, Neurocognit Dev Unit, London WC1N 1EH, England
关键词
genotype; phenotype; Fragile X syndrome; Williams syndrome; mouse models; quantitative genetics; molecular genetics; computational models;
D O I
10.1002/dev.10035
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this article, the discuss the complex problem of relating genotype to phenotype and challenge the simple mapping of genes to higher level cognitive modules. We examine various methods that have been used to investigate this relation including quantitative genetics, molecular genetics, animal models, and in-depth psychological and computational studies of developmental disorders. Both single gene and multiple gene disorders indicate that the relationship between genotype and phenotype is very indirect and that, rather than identifying mere snapshots of developmental outcomes, the process of ontogenetic development itself must be taken into account. (C) 2002 Wiley Periodicals, Inc.
引用
收藏
页码:311 / 322
页数:12
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