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Disease Gene Mapping in Isolated Human Populations: the Example of Finland

Overview
Journal J Med Genet
Specialty Genetics
Date 1993 Oct 1
PMID 8230163
Citations 99
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References
1.
Cavalli-Sforza L . Genes, peoples and languages. Sci Am. 1991; 265(5):104-10. DOI: 10.1038/scientificamerican1191-104. View

2.
Schwartz M, Rosenberg T, van den Hurk J, van de Pol D, Cremers F . Identification of mutations in Danish choroideremia families. Hum Mutat. 1993; 2(1):43-7. DOI: 10.1002/humu.1380020108. View

3.
Meretoja J . Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. A previously unrecognized heritable syndrome. Ann Clin Res. 1969; 1(4):314-24. View

4.
Kere J, Norio R, Savilahti E, Estivill X, de la Chapelle A . Cystic fibrosis in Finland: a molecular and genealogical study. Hum Genet. 1989; 83(1):20-5. DOI: 10.1007/BF00274141. View

5.
Alitalo T, Kruse T, de la Chapelle A . Refined localization of the gene causing X-linked juvenile retinoschisis. Genomics. 1991; 9(3):505-10. DOI: 10.1016/0888-7543(91)90417-d. View