X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (3907) 3907
Publication (328) 328
Book / eBook (72) 72
Newspaper Article (32) 32
Book Chapter (28) 28
Book Review (23) 23
Newsletter (22) 22
Dissertation (7) 7
Conference Proceeding (4) 4
Data Set (1) 1
Paper (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (3287) 3287
female (1889) 1889
male (1745) 1745
oncology (1163) 1163
genetics & heredity (1112) 1112
index medicus (1094) 1094
chromosome aberrations (1024) 1024
adult (1018) 1018
middle aged (996) 996
aged (829) 829
chromosomes (722) 722
karyotyping (666) 666
cancer (652) 652
genetic aspects (643) 643
chromosomes, human, pair 9 (606) 606
chromosome deletion (604) 604
comparative genomic hybridization (575) 575
in situ hybridization, fluorescence (527) 527
research (521) 521
tumors (513) 513
mutation (497) 497
genetics (491) 491
loss of heterozygosity (491) 491
chromosome mapping (481) 481
chromosomes, human, pair 9 - genetics (470) 470
child (442) 442
genes (427) 427
pathology (392) 392
adolescent (385) 385
cell biology (364) 364
gene (364) 364
cytogenetics (350) 350
expression (348) 348
prognosis (344) 344
child, preschool (343) 343
aged, 80 and over (342) 342
phenotype (323) 323
animals (321) 321
polymerase chain reaction (309) 309
infant (299) 299
research article (299) 299
mutations (297) 297
genomes (295) 295
translocation, genetic (291) 291
heterozygosity (284) 284
genomics (273) 273
nucleic acid hybridization (273) 273
gene expression (271) 271
risk factors (271) 271
analysis (269) 269
biochemistry & molecular biology (259) 259
deletion (259) 259
dna (255) 255
chromosome banding (254) 254
microsatellite repeats (244) 244
gene deletion (242) 242
trisomy (240) 240
dna, neoplasm - genetics (236) 236
hematology (234) 234
abnormalities, multiple - genetics (230) 230
chromosome 9 (228) 228
alleles (223) 223
hybridization (223) 223
carcinoma, squamous cell - genetics (222) 222
medicine (221) 221
abnormalities (217) 217
genetic markers (217) 217
in-situ hybridization (214) 214
diagnosis (211) 211
deoxyribonucleic acid--dna (208) 208
chromosome disorders (201) 201
base sequence (199) 199
infant, newborn (188) 188
pedigree (187) 187
multidisciplinary sciences (186) 186
amplification (184) 184
identification (182) 182
molecular sequence data (182) 182
cytogenetic analysis (179) 179
tumor-suppressor gene (179) 179
carcinoma (177) 177
clinical neurology (174) 174
health aspects (173) 173
genotype (170) 170
article (167) 167
gene amplification (167) 167
genetic predisposition to disease (166) 166
copy number (163) 163
brain neoplasms - genetics (161) 161
gene dosage (160) 160
genes, tumor suppressor (158) 158
polymorphism, single nucleotide (158) 158
development and progression (154) 154
chromosome 9p (153) 153
chromosomes, human, 6-12 and x (153) 153
science (153) 153
chromosome aberrations - genetics (151) 151
lung neoplasms - genetics (151) 151
studies (151) 151
dna methylation (150) 150
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (58) 58
Collection Dvlpm't (Acquisitions) - Closed Orders (8) 8
UofT at Mississauga - Stacks (7) 7
UTL at Downsview - May be requested (6) 6
UofT at Scarborough - Stacks (5) 5
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
Gerstein Science - Reference (2) 2
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (2) 2
UofT at Scarborough - Withdrawn (2) 2
Dentistry (Harry R Abbott) - Withdrawn (1) 1
Holland Bloorview Kids Rehabilitation - Reference (1) 1
Humber River Regional Hospital - Finch Stacks (1) 1
Lakeridge Health Sciences - Oshawa (1) 1
Mathematical Sciences - Stacks (1) 1
Online Resources - Online (1) 1
Robarts - Stacks (1) 1
Royal Ontario Museum - Stacks (1) 1
Scarborough Hospital - General (1) 1
St Josephs Health Centre - Stacks (1) 1
UofT at Scarborough - Sunnybrook Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3943) 3943
Chinese (36) 36
French (20) 20
Spanish (20) 20
German (15) 15
Japanese (10) 10
Italian (9) 9
Russian (8) 8
Korean (5) 5
Danish (3) 3
Polish (3) 3
Arabic (2) 2
Croatian (2) 2
Turkish (2) 2
Dutch (1) 1
Hungarian (1) 1
Latin (1) 1
Ukrainian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Neuron, ISSN 0896-6273, 10/2011, Volume 72, Issue 2, pp. 245 - 256
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 02/2011, Volume 82, Issue 2, pp. 196 - 203
Journal Article
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, ISSN 1552-4825, 06/2018, Volume 176, Issue 6, pp. 1416 - 1422
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 11/2011, Volume 155, Issue 11, pp. 2754 - 2761
We report on a 17‐year‐old patient with midline defects, ocular hypertelorism, neuropsychomotor development delay, neonatal macrosomy, and dental anomalies.... 
array‐CGH | multiple congenital anomalies | chromosomal aberration | midline | monosomy 9p | trisomy 20p | Chromosomal aberration | Array-CGH | Trisomy 20p | Multiple congenital anomalies | Midline | Monosomy 9p | TRANSLOCATION | MIDLINE FACIAL DEFECTS | DELETION 9P | array-CGH | REGION | DISTAL 9P | GENETICS & HEREDITY | FRONTONASAL MALFORMATION | HYPERTELORISM | ARM | HYPOSPADIAS | FEMALE SEX REVERSAL | Humans | Child, Preschool | Male | Developmental Disabilities - genetics | Abnormal Karyotype | DNA Copy Number Variations | Intellectual Disability - genetics | Inheritance Patterns | Chromosomes, Human, Pair 9 - genetics | Developmental Disabilities - pathology | Metaphase | Trisomy - pathology | Chromosome Deletion | Guanine Nucleotide Exchange Factors - genetics | Intellectual Disability - pathology | In Situ Hybridization, Fluorescence | Chromosome Mapping | Comparative Genomic Hybridization - methods | Forkhead Transcription Factors - genetics | Trisomy - diagnosis | Trisomy - genetics | Adolescent | Physical Examination | Genome, Human | Chromosomes, Human, Pair 20 - genetics | Neonates | Trisomy | Bone morphogenetic protein 2 | Genomes | Bacterial artificial chromosomes | MKKS protein | DNA | gene duplication | Fluorescence in situ hybridization | chromosome 20 | Development | genomics | Gene mapping | copy number | Monosomy
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 06/2018, Volume 176, Issue 6, pp. 1416 - 1422
Journal Article
Brain, ISSN 0006-8950, 2012, Volume 135, Issue 3, pp. 709 - 722
Journal Article
Journal Article
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 3/2012, Volume 123, Issue 3, pp. 409 - 417
Journal Article