X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (891) 891
Publication (217) 217
Book Review (13) 13
Book Chapter (12) 12
Conference Proceeding (1) 1
Data Set (1) 1
Dissertation (1) 1
Journal / eJournal (1) 1
Paper (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (657) 657
index medicus (488) 488
female (457) 457
fragile x syndrome - genetics (432) 432
premutation (401) 401
fragile x mental retardation protein - genetics (393) 393
male (382) 382
fragile x syndrome (329) 329
genetics & heredity (288) 288
adult (263) 263
mutation (252) 252
middle aged (227) 227
alleles (201) 201
neurosciences (194) 194
cgg repeat (187) 187
fmr1 (186) 186
premutation carriers (174) 174
article (170) 170
aged (167) 167
fragile x mental retardation protein (166) 166
fxtas (158) 158
tremor/ataxia syndrome (157) 157
carriers (150) 150
gene (150) 150
fmr1 premutation (149) 149
clinical neurology (148) 148
fragile-x-syndrome (145) 145
phenotype (141) 141
tremor (140) 140
heterozygote (135) 135
congenital, hereditary, and neonatal diseases and abnormalities (134) 134
premature ovarian failure (134) 134
fragile x syndrome - diagnosis (129) 129
males (128) 128
fmr1 gene (126) 126
mental retardation (124) 124
ataxia (120) 120
ataxia - genetics (120) 120
fragile-x premutation (117) 117
tremor - genetics (115) 115
nervous system diseases (114) 114
prevalence (113) 113
full mutation (107) 107
genetics (105) 105
fragile x (103) 103
population (103) 103
adolescent (98) 98
women (95) 95
instability (94) 94
fmr1 messenger-rna (93) 93
obstetrics & gynecology (93) 93
primary ovarian insufficiency - genetics (93) 93
animals (92) 92
trinucleotide repeat expansion (89) 89
trinucleotide repeat expansion - genetics (89) 89
trinucleotide repeats (88) 88
tremor/ataxia syndrome fxtas (87) 87
messenger-rna (86) 86
nerve tissue proteins - genetics (86) 86
child (85) 85
fragile x syndrome - complications (85) 85
analysis (81) 81
fragile x syndrome - physiopathology (80) 80
autism (78) 78
diagnosis (78) 78
fragile x syndrome - pathology (78) 78
intranuclear inclusions (77) 77
expression (76) 76
fragile x premutation (76) 76
genetic testing (75) 75
genetic aspects (74) 74
neurology (72) 72
research (71) 71
mental illness (70) 70
biochemistry & molecular biology (67) 67
expanded alleles (65) 65
females (65) 65
pregnancy (64) 64
young adult (64) 64
age (63) 63
mental-retardation (62) 62
mutation - genetics (61) 61
reproductive biology (61) 61
pedigree (59) 59
risk factors (59) 59
expansion (58) 58
fragile x mental retardation protein - metabolism (58) 58
rna (58) 58
mouse model (57) 57
psychiatry (57) 57
rna-binding proteins (57) 57
methylation (56) 56
aged, 80 and over (55) 55
gene expression (54) 54
cgg-repeat (53) 53
dna methylation (53) 53
fmrp (52) 52
fragile x syndrome - psychology (52) 52
full-mutation (52) 52
genotype (52) 52
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (882) 882
Spanish (9) 9
French (5) 5
German (2) 2
Korean (2) 2
Polish (2) 2
Czech (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Clinical Genetics, ISSN 0009-9163, 04/2010, Volume 77, Issue 4, pp. 374 - 381
Journal Article
Experimental Brain Research, ISSN 0014-4819, 9/2019, Volume 237, Issue 9, pp. 2269 - 2278
Journal Article
Journal Article
Genes, Brain and Behavior, ISSN 1601-1848, 07/2012, Volume 11, Issue 5, pp. 577 - 585
Journal Article
Journal Article
The Cerebellum, ISSN 1473-4222, 10/2016, Volume 15, Issue 5, pp. 587 - 594
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2017, Volume 55, pp. 11 - 19
Journal Article
Neuropsychologia, ISSN 0028-3932, 12/2012, Volume 50, Issue 14, pp. 3757 - 3763
Neuropsychological investigations of FMR1 premutation carriers without FXTAS present one domain resulting in contradictory findings, namely that of... 
Fragile X permutation | Numbers | Calculation | Visuo-spatial system | DYSCALCULIA | LEARNING-DISABILITY | FRAGILE-X PREMUTATION | PHENOTYPES | TURNER-SYNDROME | NEUROSCIENCES | PSYCHOLOGY, EXPERIMENTAL | CHILDREN | BASAL GANGLIA DYSFUNCTION | BEHAVIORAL SCIENCES | AMYGDALA DYSFUNCTION | DEFICITS | PRADER-WILLI-SYNDROME | Genetics | Females |