-
1
-
-
0001836958
-
X-linked mental retardation and the fragile X syndrome: A clinical approach
-
Davies KE, ed. Oxford: Oxford University Press
-
Fryns JP. X-linked mental retardation and the fragile X syndrome: a clinical approach. In: Davies KE, ed. The fragile X syndrome. Oxford: Oxford University Press, 1989.
-
(1989)
The Fragile x Syndrome
-
-
Fryns, J.P.1
-
2
-
-
0001966753
-
Physical and behavioural phenotype
-
Hagerman RJ, Cronister A, eds. Baltimore: The Johns Hopkins University Press
-
Hagerman RJ. Physical and behavioural phenotype. In: Hagerman RJ, Cronister A, eds. Fragile-X syndrome: diagnosis, treatment and research. Baltimore: The Johns Hopkins University Press, 1996.
-
(1996)
Fragile-X Syndrome: Diagnosis, Treatment and Research
-
-
Hagerman, R.J.1
-
4
-
-
0025305112
-
The female and the fragile X syndrome: Data on clinical and psychological findings in 7 fra(X) carriers
-
Borghgraef M, Fryns JP, van den Berghe H. The female and the fragile X syndrome: data on clinical and psychological findings in 7 fra(X) carriers. Clin Genet 1990;37:341-6.
-
(1990)
Clin Genet
, vol.37
, pp. 341-346
-
-
Borghgraef, M.1
Fryns, J.P.2
Van den Berghe, H.3
-
5
-
-
0002281483
-
The treatment of emotional and behavioral problems
-
Hagerman RJ, Cronister A, eds. Baltimore: The Johns Hopkins University Press
-
Sobesky W. The treatment of emotional and behavioral problems. In: Hagerman RJ, Cronister A, eds. Fragile-X syndrome: diagnosis, treatment and research. Baltimore: The Johns Hopkins University Press, 1996.
-
(1996)
Fragile-X Syndrome: Diagnosis, Treatment and Research
-
-
Sobesky, W.1
-
6
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk AJ, Pieretti M, Sutcliffe JS, et al. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 1991;65:905-14.
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.1
Pieretti, M.2
Sutcliffe, J.S.3
-
7
-
-
0026347628
-
Fragile X genotype characterized by an unstable region of DNA
-
Yu S, Pritchard M, Kremer E, et al. Fragile X genotype characterized by an unstable region of DNA. Science 1991;252:1179-81.
-
(1991)
Science
, vol.252
, pp. 1179-1181
-
-
Yu, S.1
Pritchard, M.2
Kremer, E.3
-
8
-
-
0026339303
-
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
-
Oberle I, Rousseau F, Heitz D, et al. Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome. Science 1991;252:1097-102.
-
(1991)
Science
, vol.252
, pp. 1097-1102
-
-
Oberle, I.1
Rousseau, F.2
Heitz, D.3
-
9
-
-
0026345716
-
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
-
Fu YH, Kuhl DP, Pizzuti A, et al. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox. Cell 1991;67:1047-58.
-
(1991)
Cell
, vol.67
, pp. 1047-1058
-
-
Fu, Y.H.1
Kuhl, D.P.2
Pizzuti, A.3
-
10
-
-
0025952727
-
Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation
-
Rousseau F, Heitz D, Biancalana V, et al. Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation. N Engl J Med 1991;325:1673-81.
-
(1991)
N Engl J Med
, vol.325
, pp. 1673-1681
-
-
Rousseau, F.1
Heitz, D.2
Biancalana, V.3
-
11
-
-
0026354010
-
Selection in blood cells from female carriers of the fragile X syndrome: Inverse correlation between age and proportion of active X chromosomes carrying the full mutation
-
Rousseau F, Heitz D, Oberle I, Mandel JL. Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation. J Med Genet 1991;28:830-6.
-
(1991)
J Med Genet
, vol.28
, pp. 830-836
-
-
Rousseau, F.1
Heitz, D.2
Oberle, I.3
Mandel, J.L.4
-
12
-
-
0028283366
-
Prediction of mental status in carriers of the fragile X mutation using CGG repeat length
-
Smits A, Smeets D, Hamel B, Dreesen J, de Haan A, van Oost B. Prediction of mental status in carriers of the fragile X mutation using CGG repeat length. Am J Med Genet 1994;51:497-500.
-
(1994)
Am J Med Genet
, vol.51
, pp. 497-500
-
-
Smits, A.1
Smeets, D.2
Hamel, B.3
Dreesen, J.4
De Haan, A.5
Van Oost, B.6
-
13
-
-
84942951309
-
Molecular predictors of cognitive involvement in female carriers of fragile X syndrome
-
Taylor AK, Safanda JF, Fall MZ, et al. Molecular predictors of cognitive involvement in female carriers of fragile X syndrome. JAMA 1994;271:507-14.
-
(1994)
JAMA
, vol.271
, pp. 507-514
-
-
Taylor, A.K.1
Safanda, J.F.2
Fall, M.Z.3
-
14
-
-
19144366486
-
Mental status of females with an FMR1 gene full mutation
-
De Vries BB, Wiegers AM, Smits AP, et al. Mental status of females with an FMR1 gene full mutation. Am J Hum Genet 1996;58:1025-32.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1025-1032
-
-
De Vries, B.B.1
Wiegers, A.M.2
Smits, A.P.3
-
17
-
-
0003122030
-
The necessary and sufficient conditions of therapeutic personality change
-
Kirschenbaum H, Henderson VL, eds. London: Constable
-
Rogers C. The necessary and sufficient conditions of therapeutic personality change. In: Kirschenbaum H, Henderson VL, eds. The Carl Rogers Readers. London: Constable, 1989.
-
(1989)
The Carl Rogers Readers
-
-
Rogers, C.1
-
18
-
-
0030868986
-
Psychological aspects of genetic counseling. XI. Nondirectiveness revisited
-
Kessler S. Psychological aspects of genetic counseling. XI. Nondirectiveness revisited. Am J Med Genet 1997;72:164-71.
-
(1997)
Am J Med Genet
, vol.72
, pp. 164-171
-
-
Kessler, S.1
-
19
-
-
0039077924
-
Chronic illness and the family life cycle
-
Carter B, McGoldrick M, eds. London: Allyn and Bacon
-
Rolland JS. Chronic illness and the family life cycle. In: Carter B, McGoldrick M, eds. The changing family life cycle. London: Allyn and Bacon, 1989.
-
(1989)
The Changing Family Life Cycle
-
-
Rolland, J.S.1
-
20
-
-
0038006047
-
The impact of death and serious illness on the family life cycle
-
Carter B, McGoldrick M, eds. London: Allyn and Bacon
-
Brown FH. The impact of death and serious illness on the family life cycle. In: Carter B, McGoldrick M, eds. The changing family life cycle. London: Allyn and Bacon, 1989.
-
(1989)
The Changing Family Life Cycle
-
-
Brown, F.H.1
-
21
-
-
0030972226
-
Developmental tasks of childhood and adolescence: Implications for genetic testing
-
Fanos JH. Developmental tasks of childhood and adolescence: implications for genetic testing. Am J Med Genet 1997;71:22-8.
-
(1997)
Am J Med Genet
, vol.71
, pp. 22-28
-
-
Fanos, J.H.1
|