X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (10984) 10984
Publication (1900) 1900
Newsletter (1571) 1571
Book Chapter (336) 336
Newspaper Article (159) 159
Book Review (102) 102
Dissertation (75) 75
Conference Proceeding (61) 61
Magazine Article (53) 53
Book / eBook (42) 42
Web Resource (19) 19
Reference (17) 17
Report (9) 9
Government Document (8) 8
Data Set (4) 4
Streaming Video (4) 4
Trade Publication Article (4) 4
Journal / eJournal (3) 3
Video Recording (2) 2
Paper (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (6936) 6936
fragile x syndrome (5916) 5916
male (4133) 4133
index medicus (3692) 3692
female (3535) 3535
fragile x syndrome - genetics (3452) 3452
fragile-x-syndrome (2865) 2865
animals (2492) 2492
neurosciences (2212) 2212
genetics & heredity (2172) 2172
autism (1982) 1982
research (1958) 1958
child (1745) 1745
mental retardation (1638) 1638
fragile x mental retardation protein - genetics (1577) 1577
adult (1566) 1566
medical research (1527) 1527
mutation (1509) 1509
medicine, experimental (1454) 1454
mice (1330) 1330
fragile x mental retardation protein (1290) 1290
adolescent (1264) 1264
article (1179) 1179
genetic aspects (1153) 1153
fragile x syndrome - diagnosis (1143) 1143
biochemistry & molecular biology (1133) 1133
phenotype (1024) 1024
analysis (1014) 1014
child, preschool (1007) 1007
children (974) 974
mouse model (893) 893
mental-retardation (857) 857
mental-retardation protein (853) 853
nerve tissue proteins - genetics (850) 850
gene (815) 815
middle aged (813) 813
congenital, hereditary, and neonatal diseases and abnormalities (788) 788
genetics (777) 777
intellectual disability - genetics (776) 776
clinical neurology (773) 773
reports (748) 748
mental illness (705) 705
psychiatry (686) 686
pedigree (676) 676
proteins (674) 674
fmr1 (672) 672
fragile x (671) 671
disease models, animal (670) 670
fragile x syndrome - physiopathology (669) 669
fragile x syndrome - psychology (668) 668
expression (657) 657
fragile-x (657) 657
males (647) 647
fragile x mental retardation protein - metabolism (643) 643
cgg repeat (635) 635
rna-binding proteins (620) 620
cell biology (616) 616
alleles (603) 603
synaptic plasticity (602) 602
brain (601) 601
pediatrics (601) 601
dna (584) 584
messenger-rna (580) 580
neurons (577) 577
fragile x syndrome - complications (573) 573
mice, knockout (572) 572
nervous system diseases (572) 572
diagnosis (554) 554
behavior (547) 547
heterozygote (526) 526
instability (522) 522
x chromosome (521) 521
base sequence (519) 519
intellectual disability (517) 517
molecular sequence data (517) 517
trinucleotide repeats (517) 517
methylation (515) 515
fragile x syndrome - pathology (514) 514
fmrp (504) 504
genes (502) 502
gene expression (499) 499
fragile x syndrome - metabolism (491) 491
genetic disorders (490) 490
rehabilitation (481) 481
aged (476) 476
fmr1 gene (464) 464
pregnancy (449) 449
intellectual disabilities (446) 446
prevalence (444) 444
dna methylation (436) 436
premutation (432) 432
polymerase chain reaction (419) 419
rna (414) 414
neurology (410) 410
risk factors (400) 400
rna, messenger - metabolism (394) 394
identification (393) 393
physiological aspects (384) 384
rna-binding proteins - genetics (383) 383
infant (380) 380
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (21) 21
Online Resources - Online (17) 17
Collection Dvlpm't (Acquisitions) - Vendor file (3) 3
Holland Bloorview Kids Rehabilitation - Stacks (3) 3
Collection Dvlpm't (Acquisitions) - Closed Orders (2) 2
OISE - Stacks (2) 2
UTL at Downsview - May be requested (2) 2
UofT at Mississauga - Stacks (2) 2
Gerstein Science - Theses (1) 1
Lakeridge Health Sciences - Oshawa (1) 1
Media Commons - Audio Visual (1) 1
OISE - Theses (1) 1
Robarts - Stacks (1) 1
Scarborough Hospital - General (1) 1
Scarborough Hospital - Online (1) 1
St. Michael's Hospital - Stacks (1) 1
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (1) 1
Thomas Fisher Rare Book - May be requested at Fisher (1) 1
UofT Schools - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (12479) 12479
Spanish (184) 184
French (150) 150
German (63) 63
Chinese (55) 55
Japanese (44) 44
Russian (40) 40
Portuguese (20) 20
Polish (17) 17
Dutch (16) 16
Czech (13) 13
Italian (11) 11
Korean (11) 11
Swedish (10) 10
Danish (8) 8
Hungarian (6) 6
Turkish (6) 6
Finnish (5) 5
Norwegian (5) 5
Croatian (4) 4
Hebrew (4) 4
Ukrainian (3) 3
Latvian (1) 1
Persian (1) 1
Romanian (1) 1
Serbian (1) 1
Slovak (1) 1
Slovenian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


2013, ISBN 9780888014467, 404
Book
2007, ISBN 9781600212819, x, 144
Book
11/2013
Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by impairments in social interaction and communication as well as ritualistic... 
Fragile X Syndrome | Autism Spectrum Disorder | 0317
Dissertation
Molecular diagnosis and genetic counseling for fragile X mental retardation, 01/2004
The fragile X syndrome is the most frequent cause of inherited mental retardation. It is caused by a dynamic mutation: the progressive expansion of polymorphic... 
Neurology | ni04011 Fragile X mental retardation, Genetic Counseling, Mutation, Premutation
Journal
Science Signaling, ISSN 1945-0877, 11/2017, Volume 10, Issue 504, p. eaar3825
Journal Article
by Cheng, Y and Jin, P
BIOLOGICAL PSYCHIATRY, ISSN 0006-3223, 08/2019, Volume 86, Issue 4, pp. 253 - 254
Journal Article
Nature neuroscience, ISSN 1097-6256, 01/2019, Volume 22, Issue 1, pp. 143 - 143
The original and corrected Acknowledgements are shown in the accompanying Author Correction. 
Parvalbumin | Mental retardation | Fragile X syndrome
Journal Article
2014
James Colburn was born with Fragile X Syndrome. At 26, he is a child at heart who finds joy in the smallest things and uses his gift of comedic timing to... 
Fragile X syndrome
Web Resource
Nature Reviews Drug Discovery, ISSN 1474-1776, 03/2018, Volume 17, Issue 4, p. 240
Journal Article
Fragile X screening for FRAXA and FRAXE mutations using PCR based studies: Results of a five year study, 12/2006
Background: Fragile X syndrome is the most common cause of inherited X-linked mental retardation. It is due to a mutation in a gene on X chromosome leading to... 
Fragile X syndrome, trinucleotide repeat, methylation, pre-mutation, full mutation, heterozygosity, polymerase chain reaction
Journal
Molecular analysis of fragile X syndrome in Antalya Province, 12/2005
Background: Detection of the (CGG)n repeats in the FMR1 gene that cause the fragile X syndrome (FXS), has become a milestone for phenotype-genotype correlation... 
Antalya, CGG repeats, expand long PCR, fragile X syndrome, FMR1 gene
Journal
Neuron, ISSN 0896-6273, 04/2012, Volume 74, Issue 1, p. 1
Treatment for fragile X syndrome and related autism spectrum disorders has long been thought to be effective only during a narrow window early in development.... 
Fragile X syndrome
Journal Article
Obstetrics and Gynecology, ISSN 0029-7844, 2017, Volume 129, Issue 3, pp. e41 - e55
Carrier screening is a term used to describe genetic testing that is performed on an individual who does not have any overt phenotype for a genetic disorder... 
FRAGILE-X-SYNDROME | PREVALENCE | SPINAL MUSCULAR-ATROPHY | DISEASE | PRENATAL-DIAGNOSIS | OBSTETRICS & GYNECOLOGY
Journal Article
European journal of medical genetics, ISSN 1769-7212, 09/2019, p. 103763
Journal Article
2016, Second edition., ISBN 3319338986
Web Resource
Research in Developmental Disabilities, ISSN 0891-4222, 11/2017, Volume 70, p. 113
There have been discrepancies reported in visuo-spatial construction ability in children with Autism Spectrum Disorders (ASD), fragile X Syndrome (FXS) and... 
Autism | Analysis | Fragile X syndrome | Comorbidity
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.