X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (187) 187
Publication (13) 13
Book Chapter (6) 6
Book / eBook (3) 3
Conference Proceeding (1) 1
Magazine Article (1) 1
Newspaper Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (102) 102
female (74) 74
male (66) 66
index medicus (62) 62
genetics & heredity (49) 49
adult (41) 41
mutation (36) 36
middle aged (30) 30
fragile x syndrome - genetics (23) 23
child (22) 22
phenotype (22) 22
spain (20) 20
aged (19) 19
genes (18) 18
genetic aspects (18) 18
intellectual disability - genetics (18) 18
fragile x mental retardation protein - genetics (17) 17
fragile x syndrome (17) 17
adolescent (15) 15
diagnosis (14) 14
gene (14) 14
mental retardation (14) 14
alleles (13) 13
expression (13) 13
genetics (13) 13
neurosciences (13) 13
colorectal cancer (12) 12
dna mutational analysis (12) 12
genetic testing (12) 12
heterozygote (12) 12
mutations (12) 12
risk factors (12) 12
autism (11) 11
cancer (11) 11
intellectual disabilities (11) 11
oncology (11) 11
pedigree (11) 11
analysis (10) 10
biochemistry & molecular biology (10) 10
child, preschool (10) 10
clinical neurology (10) 10
fragile x mental retardation protein (10) 10
population (10) 10
research (10) 10
aged, 80 and over (9) 9
carriers (9) 9
chromosome aberrations (9) 9
càncer colorectal (9) 9
fragile-x-syndrome (9) 9
fxtas (9) 9
genotype (9) 9
in situ hybridization, fluorescence (9) 9
mental-retardation (9) 9
cribratge (8) 8
dna (8) 8
genetic predisposition to disease (8) 8
genetic predisposition to disease - genetics (8) 8
instability (8) 8
males (8) 8
medical screening (8) 8
medicine, research & experimental (8) 8
molecular genetics (8) 8
molecular sequence data (8) 8
mosaicism (8) 8
nerve tissue proteins - genetics (8) 8
neurology (8) 8
polymerase chain reaction (8) 8
premutation (8) 8
prenatal diagnosis (8) 8
risk (8) 8
ataxia - genetics (7) 7
base sequence (7) 7
biomedicine (7) 7
cell biology (7) 7
cgg repeat (7) 7
disease (7) 7
fmr1 gene (7) 7
fmr1 premutation (7) 7
genetic counseling (7) 7
internal medicine (7) 7
locus (7) 7
methylation (7) 7
mutation - genetics (7) 7
obstetrics & gynecology (7) 7
pregnancy (7) 7
age of onset (6) 6
article (6) 6
association (6) 6
chorionic villi sampling (6) 6
fragile-x premutation (6) 6
gene frequency (6) 6
gene mutations (6) 6
genetic research (6) 6
genomes (6) 6
genomics (6) 6
health aspects (6) 6
huntington disease - genetics (6) 6
karyotyping (6) 6
melanoma - genetics (6) 6
mental illness (6) 6
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Journal Article
Journal Article
DMM Disease Models and Mechanisms, ISSN 1754-8403, 04/2017, Volume 10, Issue 4, pp. 463 - 474
Journal Article
Journal Article
Genetics in Medicine, ISSN 1098-3600, 04/2016, Volume 18, Issue 4, pp. 378 - 385
Journal Article
Journal Article
Journal of Neurodevelopmental Disorders, ISSN 1866-1947, 01/2014, Volume 6, Issue 1, pp. 30 - 30
Changes in the fragile X mental retardation 1 gene (FMR1) have been associated with specific phenotypes, most specifically those of fragile X syndrome (FXS),... 
fragile X | FMR1 premutation | health risks | BEHAVIOR PROBLEMS | TREMOR/ATAXIA SYNDROME FXTAS | FRAGILE-X PREMUTATION | PREMATURE OVARIAN FAILURE | ANTI-MULLERIAN HORMONE | NEUROSCIENCES | CLINICAL NEUROLOGY | FULL-MUTATION | CGG REPEAT | PROTEIN EXPRESSION | CLINICAL INVOLVEMENT | EARLY MENOPAUSE | Mental illness | Genetic aspects | Review
Journal Article
International Journal of Cancer, ISSN 0020-7136, 10/2019, Volume 145, Issue 7, pp. 1970 - 1981
Journal Article
Journal Article