-
1
-
-
0027300283
-
Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain
-
ABITBOL (M.), MENINI (C.), DELEZOIDE (A.L.), RHYNER (T.), VEKEMANS (M.), MALLET (J.) : « Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain », Nat. Genet., 4, 1993, pp. 147-153.
-
(1993)
Nat. Genet.
, vol.4
, pp. 147-153
-
-
Abitbol, M.1
Menini, C.2
Delezoide, A.L.3
Rhyner, T.4
Vekemans, M.5
Mallet, J.6
-
2
-
-
0029554478
-
Quantitative brain imaging studies of fragile X syndrome
-
ABRAMS (M.T.), REISS (A.L.) : « Quantitative brain imaging studies of fragile X syndrome », Dev. Brain. Dysfunct., 8, 1995, pp. 187-198.
-
(1995)
Dev. Brain. Dysfunct.
, vol.8
, pp. 187-198
-
-
Abrams, M.T.1
Reiss, A.L.2
-
4
-
-
0028234805
-
Molecular-neurobehavioral associations in females with the fragile X full mutation
-
ABRAMS (M.T.), REISS (A.L.), FREUND (L.S.), BAUMGARTNER (T.L.), CHASE (G.A.), DENCKLA (M.B.) : « Molecular-neurobehavioral associations in females with the fragile X full mutation », Am. J. Med. Genet., 51, 1994, pp. 317-327.
-
(1994)
Am. J. Med. Genet.
, vol.51
, pp. 317-327
-
-
Abrams, M.T.1
Reiss, A.L.2
Freund, L.S.3
Baumgartner, T.L.4
Chase, G.A.5
Denckla, M.B.6
-
5
-
-
0029070562
-
Specification of the neurobehavioral phenotype in males with fragile X syndrome
-
BAUMGARTNER (T.), REISS (A.L.), FREUND (L.), ABRAMS (M.T.) : « Specification of the neurobehavioral phenotype in males with fragile X syndrome », Pediatrics, 95 (5), 1995, pp. 744-752.
-
(1995)
Pediatrics
, vol.95
, Issue.5
, pp. 744-752
-
-
Baumgartner, T.1
Reiss, A.L.2
Freund, L.3
Abrams, M.T.4
-
6
-
-
0023682497
-
Fragile X syndrome: Genetic predisposition to psychopathology
-
BREGMAN (J.D.), LECKMAN (J.F.), ORT (S.I.) : « Fragile X syndrome: genetic predisposition to psychopathology », J. Autism. Dev. Disord., 18, 1988, pp. 343-354.
-
(1988)
J. Autism. Dev. Disord.
, vol.18
, pp. 343-354
-
-
Bregman, J.D.1
Leckman, J.F.2
Ort, S.I.3
-
7
-
-
0020540895
-
Fragile (X) X-linked mental retardation I: Relationship between age and intelligence and the frequency of expression of fragile (X) (q28)
-
CHUDLEY (A.E.), KNOLL (J.), GERRARD (J.W.), SHEPEL (L.), McGAHEY (E.), ANDERSON (J.) : « Fragile (X) X-linked mental retardation I: relationship between age and intelligence and the frequency of expression of fragile (X) (q28) », Am. J. Med. Genet., 14, 1983, pp. 699-712.
-
(1983)
Am. J. Med. Genet.
, vol.14
, pp. 699-712
-
-
Chudley, A.E.1
Knoll, J.2
Gerrard, J.W.3
Shepel, L.4
McGahey, E.5
Anderson, J.6
-
8
-
-
84989743902
-
A theoretical analysis of the role of hyperarousal in the learning and behavior of fragile X males
-
COHEN (I.L.) : « A theoretical analysis of the role of hyperarousal in the learning and behavior of fragile X males », Ment. Retard. Dev. Dis. Res. Rev., 1, 1995, pp. 286-291.
-
(1995)
Ment. Retard. Dev. Dis. Res. Rev.
, vol.1
, pp. 286-291
-
-
Cohen, I.L.1
-
9
-
-
0023808833
-
Social gaze, social avoidance, and repetitive behavior in fragile X males: A controlled study
-
COHEN (I.L.), FISCH (G.S.), SUDHALTER (V.), WOLF (S.E.), HANSON (D.), HAGERMAN (R.J.), JENKINS (E.G.), BROWN (W.T.) : « Social gaze, social avoidance, and repetitive behavior in fragile X males: a controlled study », Am. J. Ment. Retard., 92, 1988, pp. 436-446.
-
(1988)
Am. J. Ment. Retard.
, vol.92
, pp. 436-446
-
-
Cohen, I.L.1
Fisch, G.S.2
Sudhalter, V.3
Wolf, S.E.4
Hanson, D.5
Hagerman, R.J.6
Jenkins, E.G.7
Brown, W.T.8
-
10
-
-
0024306238
-
Parent-child dyadic gaze patterns in fragile X males and in non-fragile X males with autistic disorder
-
COHEN (I.L.), VIETZE (P.M.), SUDHALTER (V.), JENKINS (E.C.), BROWN (W.T.) : « Parent-child dyadic gaze patterns in fragile X males and in non-fragile X males with autistic disorder », J. Child. Psychol. Psychiatry, 30, 1989, pp. 845-856.
-
(1989)
J. Child. Psychol. Psychiatry
, vol.30
, pp. 845-856
-
-
Cohen, I.L.1
Vietze, P.M.2
Sudhalter, V.3
Jenkins, E.C.4
Brown, W.T.5
-
11
-
-
0026069511
-
Effects of age and communication level on eye contact in fragile X males and non-fragile X autistic males
-
COHEN (I.L.), VIETZE (P.M.), SUDHALTER (V.), JENKINS (E.G.), BROWN (W.T.) : « Effects of age and communication level on eye contact in fragile X males and non-fragile X autistic males », Am. J. Med. Genet., 38, 1991, pp. 498-502.
-
(1991)
Am. J. Med. Genet.
, vol.38
, pp. 498-502
-
-
Cohen, I.L.1
Vietze, P.M.2
Sudhalter, V.3
Jenkins, E.G.4
Brown, W.T.5
-
13
-
-
0029549970
-
Preliminary report on cognitive and adaptive behaviors of preschool-aged males with fragile X
-
FREUND (L.S.), PEEBLES (C.D.), AYLWARD (E.), REISS (A.L.) : « Preliminary report on cognitive and adaptive behaviors of preschool-aged males with fragile X », Dev. Brain. Dysfunc., 8, 1995, pp. 242-251.
-
(1995)
Dev. Brain. Dysfunc.
, vol.8
, pp. 242-251
-
-
Freund, L.S.1
Peebles, C.D.2
Aylward, E.3
Reiss, A.L.4
-
14
-
-
0025974956
-
Cognitive profiles associated with the fra(X) syndrome in males and females
-
FREUND (L.S.), REISS (A.L.) : « Cognitive profiles associated with the fra(X) syndrome in males and females », Am. J. Med. Genet., 38, 1991, pp. 542-557.
-
(1991)
Am. J. Med. Genet.
, vol.38
, pp. 542-557
-
-
Freund, L.S.1
Reiss, A.L.2
-
15
-
-
0027511297
-
Psychiatric disorders associated with fragile X in the young female
-
FREUND (L.S.), REISS (A.L.), ABRAMS (M.T.) : « Psychiatric disorders associated with fragile X in the young female », Pediatrics, 91, 1993, pp. 321-329.
-
(1993)
Pediatrics
, vol.91
, pp. 321-329
-
-
Freund, L.S.1
Reiss, A.L.2
Abrams, M.T.3
-
16
-
-
0026520331
-
Chromosome fragility and psychopathology in obligate female carriers of the fragile X chromosome
-
FREUND (L.S.), REISS (A.L.), HAGERMAN (R.J.), VINOGRADOV (S.) : « Chromosome fragility and psychopathology in obligate female carriers of the fragile X chromosome », Arch. Gen. Psychiatry. 49, 1992, pp. 54-60.
-
(1992)
Arch. Gen. Psychiatry.
, vol.49
, pp. 54-60
-
-
Freund, L.S.1
Reiss, A.L.2
Hagerman, R.J.3
Vinogradov, S.4
-
17
-
-
0026345716
-
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
-
FU (Y.H.), KUHL (D.P.), PIZZUTI (A.), PIERETTI (M.), SUTCLIFFE (J.S.), RICHARDS (S.), VERKERK (A.J.), HOLDEN (J.J.), FENWICK (R.G.), WARREN (S.T.), OOSTRA (B.A.), NELSON (D.L.), CASKEY (C.T.) : « Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox », Cell., 67, 1991, pp. 1047-1058.
-
(1991)
Cell.
, vol.67
, pp. 1047-1058
-
-
Fu, Y.H.1
Kuhl, D.P.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
-
18
-
-
0023574902
-
Developmental Gerstmann syndrome without aphasia in the fra X syndrome
-
GRIGSBY (J.), KEMPER (M.), HAGERMAN (R.J.) : « Developmental Gerstmann syndrome without aphasia in the fra X syndrome », Neuropsychologia, 25, 1987, pp. 881-891.
-
(1987)
Neuropsychologia
, vol.25
, pp. 881-891
-
-
Grigsby, J.1
Kemper, M.2
Hagerman, R.J.3
-
19
-
-
0001966753
-
Physical and behavioral phenotype
-
R.J. Hagerman and A.C. Cronister (Eds), Baltimore, Johns Hopkins University Press
-
HAGERMAN (R.J.) : « Physical and behavioral phenotype », in : R.J. Hagerman and A.C. Cronister (Eds), Fragile X Syndrome, Baltimore, Johns Hopkins University Press, 1991, pp. 3-68.
-
(1991)
Fragile X Syndrome
, pp. 3-68
-
-
Hagerman, R.J.1
-
20
-
-
0028264043
-
High functioning fragile X males: Demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression
-
HAGERMAN (R.J.), HULL (C.E.), SAFANDA (J.F.), CARPENTER (I.), STALEY (L.W.), O'CONNOR (R.A.), SEYDEL (C.), MAZZOCCO (M.M.), SNOW (K.), THIBODEAU (S.N.) et al. : « High functioning fragile X males: demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression », Am. J. Med. Genet., 51, 1994, pp. 298-308.
-
(1994)
Am. J. Med. Genet.
, vol.51
, pp. 298-308
-
-
Hagerman, R.J.1
Hull, C.E.2
Safanda, J.F.3
Carpenter, I.4
Staley, L.W.5
O'Connor, R.A.6
Seydel, C.7
Mazzocco, M.M.8
Snow, K.9
Thibodeau, S.N.10
-
21
-
-
0026951222
-
Methylation analysis of CGG sites in the CpG island of the human FMR1 gene
-
HANSEN (R.S.), GARTLER (S.M.), SCOTT (C.R.), CHEN (S.H.), LAIRD (C.D.) : « Methylation analysis of CGG sites in the CpG island of the human FMR1 gene », Hum. Mol. Genet., 1, 1992, pp. 571-578.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 571-578
-
-
Hansen, R.S.1
Gartler, S.M.2
Scott, C.R.3
Chen, S.H.4
Laird, C.D.5
-
22
-
-
0028911332
-
Tissue-specific expression of a FMR1/beta-galactosidase fusion gene in transgenic mice
-
HERGERSBERG (M.), MATSUO (K.), GASSMANN (M.), SCHAFFNER (W.), LUSCHER (B.), RULICKE (T.), AGUZZI (A.) : « Tissue-specific expression of a FMR1/beta-galactosidase fusion gene in transgenic mice », Hum. Mol. Genet., 4 (3), 1995, pp. 359-366.
-
(1995)
Hum. Mol. Genet.
, vol.4
, Issue.3
, pp. 359-366
-
-
Hergersberg, M.1
Matsuo, K.2
Gassmann, M.3
Schaffner, W.4
Luscher, B.5
Rulicke, T.6
Aguzzi, A.7
-
23
-
-
0027397928
-
Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome
-
HINDS (H.L.), ASHLEY (C.T.), SUTCLIFFE (J.S.), NELSON (D.L.), WARREN (S.T.), HOUSMAN (D.E.), SCHALLING (M.) : « Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome », Nat. Genet., 3, 1993, pp. 36-43.
-
(1993)
Nat. Genet.
, vol.3
, pp. 36-43
-
-
Hinds, H.L.1
Ashley, C.T.2
Sutcliffe, J.S.3
Nelson, D.L.4
Warren, S.T.5
Housman, D.E.6
Schalling, M.7
-
24
-
-
0026682651
-
Mode of inheritance influences behavioral expression and molecular control of cognitive deficts in female carriers of the fragile X syndrome
-
HINTON (V.J.), DOBKIN (C.S.), HALPERIN (J.M.), JENKINS (E.C.), BROWN (W.T.), DING (X.H.), COHEN (I.L.), ROUSSEAU (R.), MIEZEJESKI (C.M.) : « Mode of inheritance influences behavioral expression and molecular control of cognitive deficts in female carriers of the fragile X syndrome », Am. J. Med. Genet., 43, 1992, pp. 87-95.
-
(1992)
Am. J. Med. Genet.
, vol.43
, pp. 87-95
-
-
Hinton, V.J.1
Dobkin, C.S.2
Halperin, J.M.3
Jenkins, E.C.4
Brown, W.T.5
Ding, X.H.6
Cohen, I.L.7
Rousseau, R.8
Miezejeski, C.M.9
-
25
-
-
84989730161
-
Analysis of FMRP, the protein deficient in fragile X syndrome
-
KERSTEN (S.), STEPHEN (T.W.) : « Analysis of FMRP, the protein deficient in fragile X syndrome », Ment. Retard. Dev. Dis. Res. Rev., 1, 1995, pp. 245-250.
-
(1995)
Ment. Retard. Dev. Dis. Res. Rev.
, vol.1
, pp. 245-250
-
-
Kersten, S.1
Stephen, T.W.2
-
26
-
-
0030059545
-
The fragile X mental retardation protein is associated with ribosomes
-
KHANDJIAN (E.W.), CORBIN (F.), WOERLY (S.), ROUSSEAU (F.) : « The fragile X mental retardation protein is associated with ribosomes », Nat. Genet., 12 (1), 1996, pp. 91-93.
-
(1996)
Nat. Genet.
, vol.12
, Issue.1
, pp. 91-93
-
-
Khandjian, E.W.1
Corbin, F.2
Woerly, S.3
Rousseau, F.4
-
28
-
-
0026772870
-
Abnormal behaviors of young girls with fragile X syndrome
-
LACHIEWICZ (A.M.) : « Abnormal behaviors of young girls with fragile X syndrome », Am. J. Med. Genet., 43, 1992, pp. 72-77.
-
(1992)
Am. J. Med. Genet.
, vol.43
, pp. 72-77
-
-
Lachiewicz, A.M.1
-
29
-
-
0028308593
-
Behavior problems of young girls with fragile X syndrome: Factor scores on the Conners' Parent's Questionnaire
-
LACHIEWICZ (A.M.), DAWSON (D.V.) : « Behavior problems of young girls with fragile X syndrome: factor scores on the Conners' Parent's Questionnaire », Am. J. Med. Genet., 51, 1994, pp. 364-369.
-
(1994)
Am. J. Med. Genet.
, vol.51
, pp. 364-369
-
-
Lachiewicz, A.M.1
Dawson, D.V.2
-
30
-
-
0030857615
-
Autistic behavior among girls with fragile X syndrome
-
MAZZOCCO (M.M.), KATES (W.R.), FREUND (L.S.), BAUMGARTNER (T.L.), REISS (A.L.) : « Autistic behavior among girls with fragile X syndrome », J. Autism. Dev. Dis., 27 (4), 1997, pp. 415-435.
-
(1997)
J. Autism. Dev. Dis.
, vol.27
, Issue.4
, pp. 415-435
-
-
Mazzocco, M.M.1
Kates, W.R.2
Freund, L.S.3
Baumgartner, T.L.4
Reiss, A.L.5
-
31
-
-
0028840859
-
Neuropsychological and psychosocial effects of the FMR-1 full mutation: Monozygotic twins discordant for the fragile X syndrome
-
MAZZOCCO (M.M.), FREUND (L.F.), BAUMGARTNER (T.L.), REISS (A.L.) : « Neuropsychological and psychosocial effects of the FMR-1 full mutation: monozygotic twins discordant for the fragile X syndrome », Neuropsychology, 9 (4), 1995, pp. 470-480.
-
(1995)
Neuropsychology
, vol.9
, Issue.4
, pp. 470-480
-
-
Mazzocco, M.M.1
Freund, L.F.2
Baumgartner, T.L.3
Reiss, A.L.4
|