Finnish Disease Heritage I: characteristics, causes, background

被引:125
作者
Norio, R [1 ]
机构
[1] Family Federat Finland, Dept Med Genet, FIN-00101 Helsinki, Finland
关键词
D O I
10.1007/s00439-002-0875-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
This review of the Finnish Disease Heritage (FDH), a group of rare hereditary diseases that are over-represented in Finland, includes the following topics: FDH characteristics, causes and background, primary theory, revis(it)ed theory, consanguineous marriages in Finland, internal migration of the 1500s, family series for further FDH studies, geography and population structure as a basis for FDH, geography of individual diseases, the structure of FDH families, family structure in individual diseases, Finnish gene mutations, linkage disequilibrium and haplotypes, age of gene mutations, frequencies of disease genes and carriers, and a short description of the possible future of FDH.
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收藏
页码:441 / 456
页数:16
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