-
6
-
-
0025744743
-
Neuropsychological, psychiatric, and physical manifestations in 149 members from 18 fragile X families
-
(1991)
American Journal of Medical Genetics
, vol.40
, pp. 234-243
-
-
Cianchetti, C.1
Sannio-Fancello, G.2
Fratta, A.L.3
Manconi, F.4
Orano, A.5
Pischedda, M.P.6
Pruna, D.7
Spinicci, G.8
Archidiacono, N.9
Filippi, G.10
-
8
-
-
0025174057
-
Neuropsychological dimensions of the fragile X syndrome: Support for a non-dominant hemisphere dysfunction hypothesis
-
(1990)
Neuropsychologia
, vol.28
, pp. 9-16
-
-
Crowe, S.1
Hay, D.2
-
9
-
-
19144366486
-
Mental status of females with an FMR1 gene full mutation
-
(1996)
American Journal of Human Genetics
, vol.58
, pp. 1025-1032
-
-
De Vries, B.B.A.1
Wiegers, A.M.2
Smits, A.P.T.3
Mohkamsing, S.4
Duivenvoorden, H.J.5
Fryns, J.-P.6
Curfs, L.M.G.7
Halley, D.J.J.8
Oostra, B.A.9
Van den Ouweland, A.M.W.10
Niermeijer, M.F.11
-
15
-
-
0026345716
-
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
-
(1991)
Cell
, vol.67
, pp. 1047-1058
-
-
Fu, Y.H.1
Kuhl, D.P.A.2
Pizzuti, A.3
Pieretti, M.4
Sutcliffe, J.S.5
Richards, S.6
Verkerk, A.J.7
Holden, J.J.8
Fenwick, R.G.9
Warren, S.T.10
Oostra, B.A.11
Nelson, D.L.12
Caskey, C.T.13
-
21
-
-
0026729635
-
K-ABC profiles in children with fragile X syndrome, Down syndrome, and nonspecific mental retardation
-
(1992)
American Journal of Mental Retardation
, vol.97
, pp. 39-46
-
-
Hodapp, R.M.1
Leckman, J.F.2
Dykens, E.M.3
Sparrow, S.4
Zelinsky, D.5
Ort, S.6
-
35
-
-
0025952727
-
Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation
-
(1991)
New England Journal of Medicine
, vol.325
, pp. 1673-1681
-
-
Rousseau, F.1
Heitz, D.2
Biancalana, B.3
Blumenfeld, S.4
Kretz, C.5
Boue, J.6
Tommerup, N.7
Van Der Hagen, C.8
DeLozier-Blanchet, C.9
Croquette, M.F.10
Gilgenkrantz, S.11
Jalbert, P.12
Voelckel, M.A.13
Oberle, I.14
Mandel, J.-L.15
-
36
-
-
0028141919
-
A multicenter study on genotype-phenotype correlations in fragile X syndrome, using direct diagnosis with probe StB 12.3: The first 2253 cases
-
(1994)
American Journal of Human Genetics
, vol.55
, pp. 225-237
-
-
Rousseau, F.1
Heitz, D.2
Tarleton, J.3
MacPherson, J.4
Malmgren, H.5
Dahl, N.6
Barnicoat, A.7
Matthew, C.8
Mornet, E.9
Teuada, I.10
Maddalene, A.11
Spiegel, R.12
Schinzel, A.13
Marcos, J.A.G.14
Schorderet, D.F.15
Schaap, T.16
Maccioni, L.17
Russo, S.18
Jacobs, P.A.19
Schwartz, C.20
Mandel, J.-L.21
more..
-
39
-
-
84942951309
-
Molecular predictors of cognitive involvement in female carriers of fragile X syndrome
-
(1994)
Journal of the American Medical Association
, vol.271
, pp. 507-514
-
-
Taylor, A.K.1
Safanda, J.F.2
Fall, M.Z.3
Quince, C.4
Lang, K.A.5
Hull, C.E.6
Carpenter, I.7
Staley, L.W.8
Hagerman, R.J.9
-
41
-
-
0028673977
-
Neurobehavioral characteristics of CGG amplification status in fragile X females
-
(1994)
American Journal of Medical Genetics
, vol.54
, pp. 378-383
-
-
Thompson, N.M.1
Gulley, M.L.2
Rogeness, G.A.3
Clayton, R.J.4
Johnson, C.5
Hazelton, B.6
Cho, C.G.7
Zellmer, V.T.8
-
42
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
(1991)
Cell
, vol.65
, pp. 904-914
-
-
Verkerk, A.J.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.H.4
Kuhl, D.P.5
Pizzuti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Zhang, F.P.10
Eussen, B.E.11
VanOmmen, G.J.B.12
Blonden, L.A.J.13
Riggins, G.J.14
Chastain, J.L.15
Kunst, C.B.16
Galjaard, H.17
Caskey, T.C.18
Nelson, D.L.19
Oostra, B.A.20
Warren, S.T.21
more..
-
47
-
-
0026347628
-
Fragile X genotype characterized by an unstable region of DNA
-
(1991)
Science
, vol.252
, pp. 1179-1181
-
-
Yu, S.1
Pritchard, M.2
Kremer, E.3
Lynch, M.4
Nancarrow, J.5
Baker, E.6
Holman, K.7
Mulley, J.C.8
Warren, S.T.9
Schlessinger, D.10
Sutherland, G.R.11
Richards, R.I.12
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