-
1
-
-
20844441928
-
FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy
-
Biancalana, V., Toft, M., Le, B. I., Tison, F., Scherrer, E., Thibodeau, S., Mandel, J. L., Brice, A., Farrer, M. J. & Durr, A. (2005) FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy. Arch Neurol 62, 962-966.
-
(2005)
Arch Neurol
, vol.62
, pp. 962-966
-
-
Biancalana, V.1
Toft, M.2
Le, B.I.3
Tison, F.4
Scherrer, E.5
Thibodeau, S.6
Mandel, J.L.7
Brice, A.8
Farrer, M.J.9
Durr, A.10
-
2
-
-
23944493381
-
FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure
-
Bretherick, K. L., Fluker, M. R. & Robinson, W. P. (2005) FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure. Hum Genet 117, 376-382.
-
(2005)
Hum Genet
, vol.117
, pp. 376-382
-
-
Bretherick, K.L.1
Fluker, M.R.2
Robinson, W.P.3
-
3
-
-
18044379515
-
Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome
-
Brown, V., Jin, P., Ceman, S., Darnell, J. C., O'Donnell, W. T., Tenenbaum, S. A., Jin, X., Feng, Y., Wilkinson, K. D., Keene, J. D., Darnell, R. B. & Warren, S. T. (2001) Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome. Cell 107, 477-487.
-
(2001)
Cell
, vol.107
, pp. 477-487
-
-
Brown, V.1
Jin, P.2
Ceman, S.3
Darnell, J.C.4
O'Donnell, W.T.5
Tenenbaum, S.A.6
Jin, X.7
Feng, Y.8
Wilkinson, K.D.9
Keene, J.D.10
Darnell, R.B.11
Warren, S.T.12
-
4
-
-
0027375451
-
Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test
-
Brown, W. T., Houck, G. E., Jr., Jeziorowska, A., Levinson, F. N., Ding, X., Dobkin, C., Zhong, N., Henderson, J., Brooks, S. S. & Jenkins, E. C. (1993) Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test. JAMA 270, 1569-1575.
-
(1993)
JAMA
, vol.270
, pp. 1569-1575
-
-
Brown, W.T.1
Houck, G.E.2
Jeziorowska, A.3
Levinson, F.N.4
Ding, X.5
Dobkin, C.6
Zhong, N.7
Henderson, J.8
Brooks, S.S.9
Jenkins, E.C.10
-
5
-
-
0029934242
-
Prenatal diagnosis and carrier screening for fragile X by PCR
-
Brown, W. T., Nolin, S., Houck, G., Jr., Ding, X., Glicksman, A., Li, S. Y., Stark-Houck, S., Brophy, P., Duncan, C., Dobkin, C. & Jenkins, E. (1996) Prenatal diagnosis and carrier screening for fragile X by PCR. Am J Med Genet 64, 191-195.
-
(1996)
Am J Med Genet
, vol.64
, pp. 191-195
-
-
Brown, W.T.1
Nolin, S.2
Houck, G.3
Ding, X.4
Glicksman, A.5
Li, S.Y.6
Stark-Houck, S.7
Brophy, P.8
Duncan, C.9
Dobkin, C.10
Jenkins, E.11
-
6
-
-
0344668735
-
The (CGG)n repeat element within the 5′ untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter
-
Chen, L. S., Tassone, F., Sahota, P. & Hagerman, P. J. (2003) The (CGG)n repeat element within the 5′ untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter. Hum Mol Genet 12, 3067-3074.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 3067-3074
-
-
Chen, L.S.1
Tassone, F.2
Sahota, P.3
Hagerman, P.J.4
-
7
-
-
0035746538
-
FMR1 and the fragile X syndrome: Human genome epidemiology review
-
Crawford, D. C., Acuna, J. M. & Sherman, S. L. (2001) FMR1 and the fragile X syndrome: Human genome epidemiology review. Genet Med 3, 359-371.
-
(2001)
Genet Med
, vol.3
, pp. 359-371
-
-
Crawford, D.C.1
Acuna, J.M.2
Sherman, S.L.3
-
8
-
-
26844510735
-
Telephone testing and teacher assessment of reading skills in 7-year-olds: I. Substantial correspondence for a sample of 5808 children and for extremes
-
Dale, P. S., Harlaar, N. & Plomin, R. (2005) Telephone testing and teacher assessment of reading skills in 7-year-olds: I. Substantial correspondence for a sample of 5808 children and for extremes. Reading and Writing: An Interdisciplinary Journal 18, 385-400.
-
(2005)
Reading and Writing: An Interdisciplinary Journal
, vol.18
, pp. 385-400
-
-
Dale, P.S.1
Harlaar, N.2
Plomin, R.3
-
9
-
-
0037084852
-
Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: Loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles
-
Dombrowski, C., Levesque, S., Morel, M. L., Rouillard, P., Morgan, K. & Rousseau, F. (2002) Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: Loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles. Hum Mol Genet 11, 371-378.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 371-378
-
-
Dombrowski, C.1
Levesque, S.2
Morel, M.L.3
Rouillard, P.4
Morgan, K.5
Rousseau, F.6
-
10
-
-
0028719882
-
Variability in early communicative development
-
Fenson, L., Dale, P. S., Reznick, J. S., Bates, E., Thal, D. J. & Pethick, S. J. (1994) Variability in early communicative development. Monogr Soc Res Child Dev 59, 1-173.
-
(1994)
Monogr Soc Res Child Dev
, vol.59
, pp. 1-173
-
-
Fenson, L.1
Dale, P.S.2
Reznick, J.S.3
Bates, E.4
Thal, D.J.5
Pethick, S.J.6
-
11
-
-
0031001074
-
DNA by mail: An inexpensive and noninvasive method for collecting DNA samples from widely dispersed populations
-
Freeman, B., Powell, J., Ball, D., Hill, L., Craig, I. & Plomin, R. (1997) DNA by mail: An inexpensive and noninvasive method for collecting DNA samples from widely dispersed populations. Behav Genet 27, 251-257.
-
(1997)
Behav Genet
, vol.27
, pp. 251-257
-
-
Freeman, B.1
Powell, J.2
Ball, D.3
Hill, L.4
Craig, I.5
Plomin, R.6
-
12
-
-
0037270487
-
DNA from buccal swabs recruited by mail: Evaluation of storage effects on long-term stability and suitability for multiplex polymerase chain reaction genotyping
-
Freeman, B., Smith, N., Curtis, C., Huckett, L., Mill, J. & Craig, I. W. (2003) DNA from buccal swabs recruited by mail: Evaluation of storage effects on long-term stability and suitability for multiplex polymerase chain reaction genotyping. Behav Genet 33, 67-72.
-
(2003)
Behav Genet
, vol.33
, pp. 67-72
-
-
Freeman, B.1
Smith, N.2
Curtis, C.3
Huckett, L.4
Mill, J.5
Craig, I.W.6
-
13
-
-
0036345801
-
Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers
-
Greco, C. M., Hagerman, R. J., Tassone, F., Chudley, A. E., Del Bigio, M. R., Jacquemont, S., Leehey, M. & Hagerman, P. J. (2002) Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers. Brain 125, 1760-1771.
-
(2002)
Brain
, vol.125
, pp. 1760-1771
-
-
Greco, C.M.1
Hagerman, R.J.2
Tassone, F.3
Chudley, A.E.4
Del Bigio, M.R.5
Jacquemont, S.6
Leehey, M.7
Hagerman, P.J.8
-
14
-
-
2342635196
-
The fragile-X premutation: A maturing perspective
-
Hagerman, P. J. & Hagerman, R. J. (2004) The fragile-X premutation: a maturing perspective. Am J Hum Genet 74, 805-816.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 805-816
-
-
Hagerman, P.J.1
Hagerman, R.J.2
-
16
-
-
21344452734
-
Biomedical advances in developmental psychology: The case of fragile X syndrome
-
Hagerman, R. J. (1996) Biomedical advances in developmental psychology: The case of fragile X syndrome. Developmental Psychology 32, 416-424.
-
(1996)
Developmental Psychology
, vol.32
, pp. 416-424
-
-
Hagerman, R.J.1
-
17
-
-
2342453253
-
Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation
-
Hagerman, R. J., Leavitt, B. R., Farzin, F., Jacquemont, S., Greco, C. M., Brunberg, J. A., Tassone, F., Hessl, D., Harris, S. W., Zhang, L., Jardini, T., Gane, L. W., Ferranti, J., Ruiz, L., Leehey, M. A., Grigsby, J. & Hagerman, P. J. (2004) Fragile-X-associated tremor/ ataxia syndrome (FXTAS) in females with the FMR1 premutation. Am J Hum Genet 74, 1051-1056.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1051-1056
-
-
Hagerman, R.J.1
Leavitt, B.R.2
Farzin, F.3
Jacquemont, S.4
Greco, C.M.5
Brunberg, J.A.6
Tassone, F.7
Hessl, D.8
Harris, S.W.9
Zhang, L.10
Jardini, T.11
Gane, L.W.12
Ferranti, J.13
Ruiz, L.14
Leehey, M.A.15
Grigsby, J.16
Hagerman, P.J.17
-
18
-
-
0035838379
-
Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X
-
Hagerman, R. J., Leehey, M., Heinrichs, W., Tassone, F., Wilson, R., Hills, J., Grigsby, J., Gage, B. & Hagerman, P. J. (2001) Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology 57, 127-130.
-
(2001)
Neurology
, vol.57
, pp. 127-130
-
-
Hagerman, R.J.1
Leehey, M.2
Heinrichs, W.3
Tassone, F.4
Wilson, R.5
Hills, J.6
Grigsby, J.7
Gage, B.8
Hagerman, P.J.9
-
19
-
-
12144289389
-
Aging in individuals with the FMR1 mutation
-
Jacquemont, S., Farzin, F., Hall, D., Leehey, M., Tassone, F., Gane, L., Zhang, L., Grigsby, J., Jardini, T., Lewin, F., Berry-Kravis, E., Hagerman, P. J. & Hagerman, R. J. (2004) Aging in individuals with the FMR1 mutation. Am J Ment Retard 109, 154-164.
-
(2004)
Am J Ment Retard
, vol.109
, pp. 154-164
-
-
Jacquemont, S.1
Farzin, F.2
Hall, D.3
Leehey, M.4
Tassone, F.5
Gane, L.6
Zhang, L.7
Grigsby, J.8
Jardini, T.9
Lewin, F.10
Berry-Kravis, E.11
Hagerman, P.J.12
Hagerman, R.J.13
-
20
-
-
0041880131
-
RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila
-
Jin, P., Zarnescu, D. C., Zhang, F., Pearson, C. E., Lucchesi, J. C., Moses, K. & Warren, S. T. (2003) RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila. Neuron 39, 739-747.
-
(2003)
Neuron
, vol.39
, pp. 739-747
-
-
Jin, P.1
Zarnescu, D.C.2
Zhang, F.3
Pearson, C.E.4
Lucchesi, J.C.5
Moses, K.6
Warren, S.T.7
-
21
-
-
0035394437
-
Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers
-
Kenneson, A., Zhang, F., Hagedorn, C. H. & Warren, S. T. (2001) Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers. Hum Mol Genet 10, 1449-1454.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1449-1454
-
-
Kenneson, A.1
Zhang, F.2
Hagedorn, C.H.3
Warren, S.T.4
-
22
-
-
0035864826
-
Evidence that fragile X mental retardation protein is a negative regulator of translation
-
Laggerbauer, B., Ostareck, D., Keidel, E. M., Ostareck-Lederer, A. & Fischer, U. (2001) Evidence that fragile X mental retardation protein is a negative regulator of translation. Hum Mol Genet 10, 329-338.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 329-338
-
-
Laggerbauer, B.1
Ostareck, D.2
Keidel, E.M.3
Ostareck-Lederer, A.4
Fischer, U.5
-
23
-
-
0035368955
-
The fragile X mental retardation protein inhibits translation via interacting with mRNA
-
Li, Z., Zhang, Y., Ku, L., Wilkinson, K. D., Warren, S. T. & Feng, Y. (2001) The fragile X mental retardation protein inhibits translation via interacting with mRNA. Nucleic Acids Res 29, 2276-2283.
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 2276-2283
-
-
Li, Z.1
Zhang, Y.2
Ku, L.3
Wilkinson, K.D.4
Warren, S.T.5
Feng, Y.6
-
25
-
-
0031297825
-
The FMR1 and FMR2 mutations are not common etiologies of academic difficulty among school-age children
-
Mazzocco, M. M., Sonna, N. L., Teisl, J. T., Pinit, A., Shapiro, B. K., Shah, N. & Reiss, A. L. (1997) The FMR1 and FMR2 mutations are not common etiologies of academic difficulty among school-age children. J Dev Behav Pediatr 18, 392-398.
-
(1997)
J Dev Behav Pediatr
, vol.18
, pp. 392-398
-
-
Mazzocco, M.M.1
Sonna, N.L.2
Teisl, J.T.3
Pinit, A.4
Shapiro, B.K.5
Shah, N.6
Reiss, A.L.7
-
26
-
-
10644267603
-
Fragile X syndrome: (What's) lost in translation?
-
Miyashiro, K. & Eberwine, J. (2004) Fragile X syndrome: (What's) lost in translation?Proc Natl Acad Sci USA 101, 17329-17330.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 17329-17330
-
-
Miyashiro, K.1
Eberwine, J.2
-
27
-
-
4544347583
-
The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy
-
Moore, C. J., Daly, E. M., Tassone, F., Tysoe, C., Schmitz, N., Ng, V., Chitnis, X., McGuire, P., Suckling, J., Davies, K. E., Hagerman, R. J., Hagerman, P. J., Murphy, K. C. & Murphy, D. G. (2004) The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy. Brain 127, 2672-2681.
-
(2004)
Brain
, vol.127
, pp. 2672-2681
-
-
Moore, C.J.1
Daly, E.M.2
Tassone, F.3
Tysoe, C.4
Schmitz, N.5
Ng, V.6
Chitnis, X.7
McGuire, P.8
Suckling, J.9
Davies, K.E.10
Hagerman, R.J.11
Hagerman, P.J.12
Murphy, K.C.13
Murphy, D.G.14
-
28
-
-
0001092066
-
The validity of a parent-based assessment of cognitive abilities in three-year olds
-
Oliver, B., Dale, P. S., Saudino, K. J., Petrill, S. A., Pike, A. & Plomin, R. (2002) The validity of a parent-based assessment of cognitive abilities in three-year olds. Early Child Development and Care 172, 337-348.
-
(2002)
Early Child Development and Care
, vol.172
, pp. 337-348
-
-
Oliver, B.1
Dale, P.S.2
Saudino, K.J.3
Petrill, S.A.4
Pike, A.5
Plomin, R.6
-
29
-
-
4544310635
-
A twin study of teacher-reported mathematics performance and low performance in 7-year olds
-
Oliver, B., Harlaar, N., Hayiou-Thomas, M. E., Kovas, Y., Walker, S. O., Petrill, S. A., Spinath, F. M., Dale, P. S. & Plomin, R. (2004) A twin study of teacher-reported mathematics performance and low performance in 7-year olds. R Journal of Educational Psychology 96, 504-517.
-
(2004)
R Journal of Educational Psychology
, vol.96
, pp. 504-517
-
-
Oliver, B.1
Harlaar, N.2
Hayiou-Thomas, M.E.3
Kovas, Y.4
Walker, S.O.5
Petrill, S.A.6
Spinath, F.M.7
Dale, P.S.8
Plomin, R.9
-
30
-
-
0021921029
-
A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation
-
Pembrey, M. E., Winter, R. M. & Davies, K. E. (1985) A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation. Am J Med Genet 21, 709-717.
-
(1985)
Am J Med Genet
, vol.21
, pp. 709-717
-
-
Pembrey, M.E.1
Winter, R.M.2
Davies, K.E.3
-
31
-
-
0036259708
-
Testing cognitive abilities by telephone in a sample of 6-to 8-year olds
-
Petrill, S. A., Rempell, J., Dale, P. S., Oliver, B. & Plomin, R. (2002) Testing cognitive abilities by telephone in a sample of 6-to 8-year olds. Intelligence 30, 353-360.
-
(2002)
Intelligence
, vol.30
, pp. 353-360
-
-
Petrill, S.A.1
Rempell, J.2
Dale, P.S.3
Oliver, B.4
Plomin, R.5
-
32
-
-
0037277998
-
Genetics, genes, genomics and g
-
Plomin, R. (2003) Genetics, genes, genomics and g. Mol Psychiatry 8, 1-5.
-
(2003)
Mol Psychiatry
, vol.8
, pp. 1-5
-
-
Plomin, R.1
-
33
-
-
18244402218
-
A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: A five-stage design using DNA pooling and extreme selected groups
-
Plomin, R., Hill, L., Craig, I. W., McGuffin, P., Purcell, S., Sham, P., Lubinski, D., Thompson, L. A., Fisher, P. J., Turic, D. & Owen, M. J. (2001) A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: A five-stage design using DNA pooling and extreme selected groups. Behav Genet 31, 497-509.
-
(2001)
Behav Genet
, vol.31
, pp. 497-509
-
-
Plomin, R.1
Hill, L.2
Craig, I.W.3
McGuffin, P.4
Purcell, S.5
Sham, P.6
Lubinski, D.7
Thompson, L.A.8
Fisher, P.J.9
Turic, D.10
Owen, M.J.11
-
34
-
-
0028340175
-
The genetic basis of complex human behaviors
-
Plomin, R., Owen, M. J. & McGuffin, P. (1994) The genetic basis of complex human behaviors. Science 264, 1733-1739.
-
(1994)
Science
, vol.264
, pp. 1733-1739
-
-
Plomin, R.1
Owen, M.J.2
McGuffin, P.3
-
35
-
-
10644243538
-
X-linked mental retardation
-
Ropers, H. H. & Hamel, B. C. (2005) X-linked mental retardation. Nat Rev Genet 6, 46-57.
-
(2005)
Nat Rev Genet
, vol.6
, pp. 46-57
-
-
Ropers, H.H.1
Hamel, B.C.2
-
36
-
-
0034522229
-
Premature ovarian failure in the fragile X syndrome
-
Sherman, S. L. (2000) Premature ovarian failure in the fragile X syndrome. Am J Med Genet 97, 189-194.
-
(2000)
Am J Med Genet
, vol.97
, pp. 189-194
-
-
Sherman, S.L.1
-
37
-
-
0037348314
-
Phenotypic 'g'early in life: On the etiology of general cognitive ability in a large population sample of twin children aged 2 to 4 years
-
Spinath, F. M., Ronald, A., Harlaar, N., Price, T. S. & Plomin, R. (2003) Phenotypic 'g'early in life: On the etiology of general cognitive ability in a large population sample of twin children aged 2 to 4 years. Intelligence 31, 195-210.
-
(2003)
Intelligence
, vol.31
, pp. 195-210
-
-
Spinath, F.M.1
Ronald, A.2
Harlaar, N.3
Price, T.S.4
Plomin, R.5
-
38
-
-
7244224871
-
Fragile X mental retardation protein is associated with translating polyribosomes in neuronal cells
-
Stefani, G., Fraser, C. E., Darnell, J. C. & Darnell, R. B. (2004) Fragile X mental retardation protein is associated with translating polyribosomes in neuronal cells. J Neurosci 24, 7272-7276.
-
(2004)
J Neurosci
, vol.24
, pp. 7272-7276
-
-
Stefani, G.1
Fraser, C.E.2
Darnell, J.C.3
Darnell, R.B.4
-
40
-
-
0034526068
-
Transcription of the FMR1 gene in individuals with fragile X syndrome
-
Tassone, F., Hagerman, R. J., Chamberlain, W. D. & Hagerman, P. J. (2000) Transcription of the FMR1 gene in individuals with fragile X syndrome. Am J Med Genet 97, 195-203.
-
(2000)
Am J Med Genet
, vol.97
, pp. 195-203
-
-
Tassone, F.1
Hagerman, R.J.2
Chamberlain, W.D.3
Hagerman, P.J.4
-
42
-
-
0036807407
-
Twins early development study (TEDS): A multivariate, longitudinal genetic investigation of language, cognition and behavior problems in childhood
-
Trouton, A., Spinath, F. M. & Plomin, R. (2002) Twins early development study (TEDS): A multivariate, longitudinal genetic investigation of language, cognition and behavior problems in childhood. Twin Res 5, 444-448.
-
(2002)
Twin Res
, vol.5
, pp. 444-448
-
-
Trouton, A.1
Spinath, F.M.2
Plomin, R.3
-
43
-
-
0029924873
-
Prevalence of fragile X syndrome
-
Turner, G., Webb, T., Wake, S. & Robinson, H. (1996) Prevalence of fragile X syndrome. Am J Med Genet 64, 196-197.
-
(1996)
Am J Med Genet
, vol.64
, pp. 196-197
-
-
Turner, G.1
Webb, T.2
Wake, S.3
Robinson, H.4
-
44
-
-
20444447397
-
Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS)
-
Van Dam, D., Errijgers, V., Kooy, R. F., Willemsen, R., Mientjes, E., Oostra, B. A. & De Deyn, P. P. (2005) Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS). Behav Brain Res 162, 233-239.
-
(2005)
Behav Brain Res
, vol.162
, pp. 233-239
-
-
Van Dam, D.1
Errijgers, V.2
Kooy, R.F.3
Willemsen, R.4
Mientjes, E.5
Oostra, B.A.6
De Deyn, P.P.7
-
45
-
-
4544257133
-
Nature, nurture and academic achievement: A twin study of teacher assessments of 7-year-olds
-
Walker, S. O., Petrill, S. A., Spinath, F. M. & Plomin, R. (2004) Nature, nurture and academic achievement: A twin study of teacher assessments of 7-year-olds. Br J Educ Psychol 74, 323-342.
-
(2004)
Br J Educ Psychol
, vol.74
, pp. 323-342
-
-
Walker, S.O.1
Petrill, S.A.2
Spinath, F.M.3
Plomin, R.4
-
47
-
-
0034130169
-
FRAXA and FRAXE: The results of a five year survey
-
Youings, S. A., Murray, A., Dennis, N., Ennis, S., Lewis, C., McKechnie, N., Pound, M., Sharrock, A. & Jacobs, P. (2000) FRAXA and FRAXE: The results of a five year survey. J Med Genet 37, 415-421.
-
(2000)
J Med Genet
, vol.37
, pp. 415-421
-
-
Youings, S.A.1
Murray, A.2
Dennis, N.3
Ennis, S.4
Lewis, C.5
McKechnie, N.6
Pound, M.7
Sharrock, A.8
Jacobs, P.9
-
48
-
-
1942467797
-
Molecular insights into mental retardation: Multiple functions for the Fragile X mental retardation protein?
-
Zalfa, F. & Bagni, C. (2004) Molecular insights into mental retardation: Multiple functions for the Fragile X mental retardation protein?Curr Issues Mol Biol 6, 73-88.
-
(2004)
Curr Issues Mol Biol
, vol.6
, pp. 73-88
-
-
Zalfa, F.1
Bagni, C.2
-
49
-
-
0035577350
-
A high density of X-linked genes for general cognitive ability: A run-away process shaping human evolution?
-
Zechner, U., Wilda, M., Kehrer-Sawatzki, H., Vogel, W., Fundele, R. & Hameister, H. (2001) A high density of X-linked genes for general cognitive ability: A run-away process shaping human evolution?Trends Genet 17, 697-701.
-
(2001)
Trends Genet
, vol.17
, pp. 697-701
-
-
Zechner, U.1
Wilda, M.2
Kehrer-Sawatzki, H.3
Vogel, W.4
Fundele, R.5
Hameister, H.6
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