References
Sherman, S.L. et al. Hum. Genet. 69, 289–299 (1985).
Verkerk, A.J.M.H. et al. Cell 65, 905–914 (1991).
Yu, S. et al. Science 252, 1179–1181 (1991).
Fu, Y-H et al. Cell 67, 1047–1058 (1991).
Kremer, E.J. et al. Science 252, 1711–1714, (1991).
Richards, R.I. et al. Nature Genet. 1, 257–260 (1992).
Haldane, J.B.S. J. Genet. 31, 317–326 (1935).
Kerem, B-S et al. Science 245, 1073–1080 (1989).
Morton, N.E. & Macpherson, J.N. Proc. natn. Acad. Sci. U.S.A. 89, 4215–4217 (1992).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Chakravarti, A. Fragile X founder effect?. Nat Genet 1, 237–238 (1992). https://doi.org/10.1038/ng0792-237
Issue Date:
DOI: https://doi.org/10.1038/ng0792-237
- Springer Nature America, Inc.
This article is cited by
-
Genetic Counseling for Fragile X Syndrome: Updated Recommendations of the National Society of Genetic Counselors
Journal of Genetic Counseling (2005)
-
Expansion to full mutation of a FMR1 intermediate allele over two generations
European Journal of Human Genetics (2004)
-
FMR1 haplotype analyses among Indians: a weak founder effect and other findings
Human Genetics (2003)
-
Trinucleotide diseases on the rise
Nature Genetics (1994)
-
Origin of the expansion mutation in myotonic dystrophy
Nature Genetics (1993)