[Chong, S.S., Eichler, E. E., Nelson, D.L., Hughes, M. R. (1994). Robust amplification and ethidium --- visible detection of the fragile X syndrome CGG repeat using Pfu polymerase. Amer. J. Med. Genet., 51, 522--526.]Search in Google Scholar
[Crawford, D.C., Acun, J.M., Sherman, S.L. (2001). FMR1 and the fragile X syndrome: Human genome epidemiology review. Genet. Med., 3, 359--371.10.1097/00125817-200109000-00006]Search in Google Scholar
[Eichler, E.E., Holden, J.J.A., Popovich, B.W., Reiss, A.L., Snow, K., Thi-bodeau, S.N., Richards, C.S., Word, P.A., Nelson, D.L. (1994). Length of uninterrupted CGG repeats determines instability in the FMR1 gene. Nat. Genet. 8, 88--94.10.1038/ng0994-88]Search in Google Scholar
[Fu, J.H., Kuhl, D.P., Pizzuti, A., Pieretti, M., Sutcliffe, J.S., Richards Verkerk, A.J., Holden, J.J., Fenwick, R.G., Jr., Warren, S.T. (1991). Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox. Cell 67, 1047--1058.10.1016/0092-8674(91)90283-5]Search in Google Scholar
[Ropers, H.H., Hamel, B.C. (2005) X-linked mental retardation. Nat. Rev. Genet. 6, 46--57.10.1038/nrg1501]Search in Google Scholar
[Turner, G., Webb, T., Wake, S., Robinson, H. (1996) Prevalence of fragile X syndrome. Amer. J. Med. Genet., 64, 196--197.10.1002/(SICI)1096-8628(19960712)64:1<196::AID-AJMG35>3.0.CO;2-G]Search in Google Scholar
[Verkerk, A.J.M.H., Pieretti, M., Suteliffe, J.S., et al. (1991) Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exibiting length variation in fragile X syndrome. Cell, 65, 905--914.]Search in Google Scholar
[Yim, S.Y., Jeon, B.H., Yang, J.A., Kim, H.J. (2008). Fragile X syndrome in Korea: A case series and a review of the literature. J. Korean Med. Sci., 23, 470--476.10.3346/jkms.2008.23.3.470]Search in Google Scholar