Author:
Filon Dvora,Faerman Marina,Smith Patricia,Oppenheim Ariella
Publisher
Springer Science and Business Media LLC
Reference15 articles.
1. Haldane, J. The rate of mutations of human genes. Hereditas suppl. 35, 267–273 (1949).
2. Angel, J.L. Porotic hyperostosis, anemias, malarias, and marshes in the prehistoric eastern Mediterranean. Science 153, 760–763 (1966).
3. Kaplan, F., Kokotsls, G., DeBraekeleer, M., Morgan, K. & Scriver, C.R. β-thalassemia genes in French-Canadians: haplotype and mutation analysis of Portneuf chromosomes. Am. J. hum. Genet. 48, 126–132 (1990).
4. Rund, D. et al. Evolution of a genetic disease In an ethnic isolate: β-thalassemia in the Jews of Kurdistan. Proc. netn. Acad. Sci. U.S.A. 88, 310–314 (1991).
5. Oppenheim, A. et al. Sporadic alleles, including a novel mutation, characterize β-thalassemia in Ashkenazi Jews. Hum. Mut. 2, 155–157 (1993).
Cited by
59 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