-
2
-
-
0014517848
-
A marker X chromosome
-
Lubs HA. A marker X chromosome. Am J Hum Genet 1969;21:231-44.
-
(1969)
Am J Hum Genet
, vol.21
, pp. 231-244
-
-
Lubs, H.A.1
-
3
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CCG repeat coincident with a fragile X break point cluster region exhibing lengh variation in fragile X syndrome
-
Verkerk AJMH, Graaff E de, De Boulle K, Eichler EE, Konecki DS, Reyniers E. et al. Identification of a gene (FMR-1) containing a CCG repeat coincident with a fragile X break point cluster region exhibing lengh variation in fragile X syndrome. Cell 1991;65:905-14.
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.M.H.1
De Graaff, E.2
De Boulle, K.3
Eichler, E.E.4
Konecki, D.S.5
Reyniers, E.6
-
5
-
-
0023275776
-
Medical progress Fragile X syndrome
-
Chudley AE, Hogerman RJ. Medical progress Fragile X syndrome. J Pediatr 1987;110:821-31.
-
(1987)
J Pediatr
, vol.110
, pp. 821-831
-
-
Chudley, A.E.1
Hogerman, R.J.2
-
7
-
-
0026649793
-
Behavional phenotype of fragile X syndrome DSM-IIIR austistic behavior in male children
-
Reiss AL, Freund L. Behavional phenotype of fragile X syndrome DSM-IIIR austistic behavior in male children. Am J Med Genet 1992;43:35-46.
-
(1992)
Am J Med Genet
, vol.43
, pp. 35-46
-
-
Reiss, A.L.1
Freund, L.2
-
8
-
-
0021295906
-
Conference report: International Workshop on the Fragile X and X-Linked Mental Retardation
-
Opitz JM, Sutherland GR. Conference report: International Workshop on the Fragile X and X-Linked Mental Retardation. Am J Med Genet 1984;17:5-94.
-
(1984)
Am J Med Genet
, vol.17
, pp. 5-94
-
-
Opitz, J.M.1
Sutherland, G.R.2
-
9
-
-
0027793938
-
Mental status and fragile X expression in relation to FMR-1 gen mutation
-
De Vries BBA, Wiegers AM, Graaff E de, Verkerk AJMH, van Hemel JO, Hally DJJ. et al. Mental status and fragile X expression in relation to FMR-1 gen mutation. Eur J Hum Genet 1993;1:72-9.
-
(1993)
Eur J Hum Genet
, vol.1
, pp. 72-79
-
-
De Vries, B.B.A.1
Wiegers, A.M.2
De Graaff, E.3
Verkerk, A.J.M.H.4
Van Hemel, J.O.5
Hally, D.J.J.6
-
10
-
-
0022227079
-
Excess thymidine induces folate sensitive fragile sites
-
Sutherland GR, Baker E, Fratim A. Excess thymidine induces folate sensitive fragile sites. Am J Med Genet 1985;22:433-43.
-
(1985)
Am J Med Genet
, vol.22
, pp. 433-443
-
-
Sutherland, G.R.1
Baker, E.2
Fratim, A.3
-
11
-
-
0025833298
-
Absence of expression of the FMR-1 gene in fragile X syndrome
-
Pieretti M, Zhang F, Fu YH, Warren ST, Oostra B A, Caskey CT, et al. Absence of expression of the FMR-1 gene in fragile X syndrome Cell 1991;66:817-22.
-
(1991)
Cell
, vol.66
, pp. 817-822
-
-
Pieretti, M.1
Zhang, F.2
Fu, Y.H.3
Warren, S.T.4
Oostra, B.A.5
Caskey, C.T.6
-
12
-
-
0026663529
-
Fifth International Workshop on the fragile X and X-linked mental retardation
-
Mandel JL, Hagerman R, Froster U, Brown, WT, Jenkins EC, Jacobs P, et al. Fifth International Workshop on the fragile X and X-linked mental retardation. Am J Med Genet 1992;43:5-27.
-
(1992)
Am J Med Genet
, vol.43
, pp. 5-27
-
-
Mandel, J.L.1
Hagerman, R.2
Froster, U.3
Brown, W.T.4
Jenkins, E.C.5
Jacobs, P.6
-
13
-
-
0026345716
-
Fragile X sites: A polymorphic and highly mutable CGG repeat in the FMR-1 gene
-
Fu YH, Kuhl DPA, Pizzulti A, Pieretti M, Richards S, Verkerk AJHM, et al: Fragile X sites: a polymorphic and highly mutable CGG repeat in the FMR-1 gene. Cell 1991;67:1047-9.
-
(1991)
Cell
, vol.67
, pp. 1047-1049
-
-
Fu, Y.H.1
Kuhl, D.P.A.2
Pizzulti, A.3
Pieretti, M.4
Richards, S.5
Verkerk, A.J.H.M.6
-
14
-
-
0021961665
-
Further segregation of the fragile X syndrome with special reference to transmitting males
-
Sherman SL, Jacobs PA, Morton NE, Froster-Iskenius U, Howard Peebles PN, Nielsen KB, et al. Further segregation of the fragile X syndrome with special reference to transmitting males. Hum Genet 1985;69:289-99.
-
(1985)
Hum Genet
, vol.69
, pp. 289-299
-
-
Sherman, S.L.1
Jacobs, P.A.2
Morton, N.E.3
Froster-Iskenius, U.4
Howard Peebles, P.N.5
Nielsen, K.B.6
|