Why do fragile X carrier frequencies differ between Asian and non-Asian populations?
Author:
Affiliation:
1. Department of Biology, Box 351800; University of Washington
2. Department of Biology, Westfield State University
3. Center on Human Development and Disability, University of Washington
Publisher
Genetics Society of Japan
Subject
Genetics,Molecular Biology,General Medicine
Reference53 articles.
1. Arinami, T., Asano, M., Kobayashi, K., Yanagi, H., and Hamaguchi, H. (1993) Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate. Hum. Genet. 92, 431–436.
2. Ashley, A. E., and Sherman, S. L. (1995) Population dynamics of a meiotic/mitotic expansion model for the fragile X syndrome. Am. J. Hum. Genet. 57, 1414–1425.
3. Barros-Núñez, P., Rosales-Reynoso, M. A., Sandoval, L., Romero-Espinoza, P., Troyo-Sanromán, R., and Ibarra, B. (2008) Genetic variation of the FMR1 gene among four Mexican populations: Mestizo, Huichol, Purepecha, and Tarahumara. Am. J. Hum. Biol. 20, 259–263.
4. Berkenstadt, M., Ries-Levavi, L., Cuckle, H., Peleg, L., and Barkai, G. (2007) Preconceptional and prenatal screening for fragile X syndrome: experience with 40,000 tests. Prenat, Diagn. 27, 991–994.
5. Bonferroni, C. (1936) Teoria statistica delle classi e calcolo delle probabilità. Pubblicazioni del R Istituto Superiore di Scienze Economiche e Commerciali di Firenze 8, 3–62.
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