Referências Bibliográficas
70
Cornish, K., C. Kogan, J. Turk, T. Manly, N. James, A. Mills e A. Dalton. The emerging
fragile X premutation phenotype: evidence from the domain of social cognition.
B Crain ogn
, v.57, n.1, Feb, p.53-60. 2005.
Crawford, D. C., J. M. Acuna e S. L. Sherman. FMR1 and the fragile X syndrome: human
genome epidemiology review. Genet Med
, v.3, n.5, Sep-Oct, p.359-71. 2001.
ford, D. C., K. L. Meadows, J. L. Newman, L. F. Taft, E. Scott, M. Leslie, L. Shubek,
P. Holmgreen,
Craw
M. Yeargin-Allsopp, C. Boyle e S. L. Sherman. Prevalence of the
fragile X syndrome in African-Americans. Am J Med Genet
, v.110, n.3, Jul 1, p.226-
33. 2002.
oulle, K., A. J. Verkerk, E. Reyniers, L. Vits, J. Hendrickx, B. Van Roy, F
e B . Van Den D
Bos, E. De Graaff, B. A. Oostra e P. J. Willems. A point mutation in the FMR-1 gene
associated with fragile X mental retardation. Nat Genet
, v.3, n.1, Jan, p.31-5. 1993.
er, E. E., J. J. Holden, B. W. Popovich, A. L. Reiss, K. Snow, S. N. Thibodeau, C. S.
Richards, P. A. Ward e D. L. Nelson. Length of uninterrupted CGG repeats
determines instability in the FMR1 gene. Nat Genet
Eichl
, v.8, n.1, Sep, p.88-94. 1994.
Eichler, E. E., S. Richards, R. A. Gibbs e D. L. Nelson. Fine structure of the human FMR1
gene. Hum Mol Genet
, v.3, n.4, Apr, p.684-5. 1994.
Farzin, F., H. Perry, D. Hessl, D. Loesch, J. Cohen, S. Bacalman, L. Gane, F. Tassone, P.
Hagerman e R. Hagerman. Autism spectrum disorders and attention-
deficit/hyperactivity disorder in boys with the fragile X premutation. J Dev Behav
Pediatr, v.27, n.2 Suppl, Apr, p.S137-44. 2006.
Y., F. Zhang, L. K. Lokey, J. L. Chastain, L. Lakkis, D. EberharFeng, t e S. T. Warren.
Translational suppression by trinucleotide repeat expansion at FMR1. Science
, v.268,
n.5211, May 5, p.731-4. 1995.
. H., D. P. Kuhl, A. Pizzuti, M. Pieretti, J. S. Sutcliffe
u, Y , S. Richards, A. J. Verkerk, J. F
J. Holden, R. G. Fenwick, Jr., S. T. Warren e Et Al. Variation of the CGG repeat at
the fragile X site results in genetic instability: resolution of the Sherman paradox.
Cell
, v.67, n.6, Dec 20, p.1047-58. 1991.
, A. M., G. Goel
acy lner, N. Juranic, S. Macura e C. T. Mcmurray. Trinucleotide repeats G
that expand in human disease form hairpin structures in vitro. Cell
, v.81, n.4, May
19, p.533-40. 1995.
e, R., D. A. Akkad, L. Arning, G. Dekomien, J. Herchenbach, E. Kunstmann, M.
Meins, S. Wieczo
Godd
rek, J. T. Epplen e S. Hoffjan. Electrophoresis of DNA in human
genetic diagnostics - state-of-the-art, alternatives and future prospects.
Electrophoresis
, v.27, n.5-6, Mar, p.939-46. 2006.