Articles

UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (13473) 13473
Book Chapter (166) 166
Dissertation (44) 44
Magazine Article (21) 21
Publication (21) 21
Book / eBook (17) 17
Newsletter (11) 11
Reference (11) 11
Web Resource (10) 10
Newspaper Article (4) 4
Conference Proceeding (3) 3
Streaming Video (3) 3
Journal / eJournal (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
mosaicism (12018) 12018
humans (9213) 9213
female (7312) 7312
science & technology (7192) 7192
life sciences & biomedicine (6824) 6824
male (5482) 5482
genetics & heredity (3383) 3383
biological and medical sciences (3264) 3264
adult (3036) 3036
animals (2783) 2783
karyotyping (2721) 2721
medical sciences (2684) 2684
pregnancy (2170) 2170
chromosome aberrations (2010) 2010
mutation (1911) 1911
phenotype (1843) 1843
child (1546) 1546
trisomy (1435) 1435
adolescent (1361) 1361
medical genetics (1319) 1319
infant, newborn (1269) 1269
child, preschool (1237) 1237
infant (1191) 1191
mice (1107) 1107
obstetrics & gynecology (1091) 1091
in situ hybridization, fluorescence (931) 931
aneuploidy (907) 907
chromosome disorders (863) 863
genetics (862) 862
mosaicism - genetics (857) 857
genetic aspects (856) 856
prenatal diagnosis (844) 844
research (843) 843
chromosomes (838) 838
fundamental and applied biological sciences. psychology (803) 803
abridged index medicus (794) 794
pedigree (768) 768
gynecology. andrology. obstetrics (763) 763
middle aged (755) 755
abnormalities, multiple - genetics (746) 746
genes (744) 744
analysis (717) 717
turner syndrome - genetics (674) 674
sex chromosomes (594) 594
research article (573) 573
genotype (571) 571
x chromosome (571) 571
alleles (562) 562
base sequence (535) 535
cytogenetics (533) 533
amniocentesis (525) 525
cell biology (525) 525
polymerase chain reaction (518) 518
dermatology (502) 502
biochemistry & molecular biology (497) 497
chromosome deletion (489) 489
sex chromosome aberrations (482) 482
syndrome (472) 472
molecular sequence data (458) 458
pediatrics (453) 453
chromosome banding (444) 444
intellectual disability - genetics (439) 439
cells, cultured (430) 430
developmental biology (424) 424
heterozygote (416) 416
translocation, genetic (416) 416
pregnancy. fetus. placenta (415) 415
genetic counseling (411) 411
down syndrome - genetics (409) 409
reproductive biology (400) 400
deoxyribonucleic acid--dna (396) 396
genomes (396) 396
neurosciences & neurology (396) 396
genetics of eukaryotes. biological and molecular evolution (370) 370
multidisciplinary sciences (363) 363
science & technology - other topics (363) 363
turner syndrome (358) 358
trisomy - genetics (348) 348
gene expression (346) 346
dna mutational analysis (343) 343
genomics (339) 339
management. prenatal diagnosis (339) 339
aged (333) 333
genetic research (331) 331
neurology (323) 323
somatic mosaicism (323) 323
chromosome aberrations - genetics (313) 313
chromosome mapping (309) 309
y chromosome (301) 301
lymphocytes (295) 295
proteins (294) 294
genetic markers (293) 293
genetic disorders (290) 290
maternal age (287) 287
risk factors (282) 282
neurosciences (280) 280
diagnosis (278) 278
gene mutations (273) 273
chimeras (272) 272
molecular and cellular biology (265) 265
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (9) 9
Online Resources - Online (7) 7
UTL at Downsview - May be requested (4) 4
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
UofT at Mississauga - Stacks (2) 2
Chemistry (A D Allen) - Stacks (1) 1
Earth Sciences (Noranda) - Stacks (1) 1
UofT at Scarborough - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (12455) 12455
French (359) 359
German (262) 262
Russian (190) 190
Spanish (156) 156
Japanese (115) 115
Italian (103) 103
Portuguese (76) 76
Polish (59) 59
Chinese (43) 43
Czech (36) 36
Hungarian (31) 31
Korean (31) 31
Romanian (18) 18
Slovak (15) 15
Dutch (11) 11
Bulgarian (5) 5
Turkish (5) 5
Danish (4) 4
Croatian (3) 3
Norwegian (3) 3
Finnish (2) 2
Serbian (2) 2
Swedish (2) 2
Catalan (1) 1
Hebrew (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


1. Full Text The categories of cutaneous mosaicism: A proposed classification
by Happle, Rudolf
American journal of medical genetics. Part A, ISSN 1552-4825, 02/2016, Volume 170, Issue 2, pp. 452 - 459
epigenetic mosaicism | superimposed segmental mosaicism of polygenic skin disorders | functional autosomal mosaicism | twin spotting | nonsegmental mosaicism | type 2 segmental mosaicism of autosomal dominant skin disorders | revertant mosaicism | segmental mosaicism of lethal autosomal mutations | patchy mosaicism without midline separation | didymosis | disseminated mosaicism | functional X‐chromosome mosaicism | type 1 segmental mosaicism of autosomal dominant skin disorders | single point mosaicism | cutaneous mosaicism | Nonsegmental mosaicism | Epigenetic mosaicism | Segmental mosaicism of lethal autosomal mutations | Single point mosaicism | Patchy mosaicism without midline separation | Didymosis | Functional X-chromosome mosaicism | Superimposed segmental mosaicism of polygenic skin disorders | Type 1 segmental mosaicism of autosomal dominant skin disorders | Functional autosomal mosaicism | Cutaneous mosaicism | Disseminated mosaicism | Twin spotting | Revertant mosaicism | Type 2 segmental mosaicism of autosomal dominant skin disorders | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Skin Diseases, Genetic - classification | Skin Diseases, Genetic - pathology | Male | Mosaicism - classification | Humans | Skin Diseases, Genetic - genetics | Epigenetic inheritance | Psoriasis | Atopic dermatitis | Analysis | Skin cancer | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text EP04.24: Confined placental mosaicism in NIPT result can account for adverse perinatal outcomes: a case report
by Yener, C and Varol, F.G and Gürkan, H and Uzun, I and Sutcu, H and Ates, S and Sayin, C.N
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 10/2019, Volume 54, Issue S1, pp. 255 - 255
Mosaicism | Placenta
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text EP02.10: Placental mosaicism and early oligohydramnios: a case report
by Sepp, K and Ustav, E
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 10/2018, Volume 52, Issue S1, pp. 199 - 199
Mosaicism | Placenta
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text EXPERIMENTAL INDUCTION OF EPIGENETIC MOSAICISM LEADS TO SUBINDIVIDUAL PHENOTYPIC HETEROGENEITY
American journal of botany, ISSN 0002-9122, 06/2019, Volume 106, Issue 6, p. 756
Heterogeneity | Mosaicism
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text VP31.06: Trisomy 16 in mosaicism
by Rodriguez, D.G and Suarez, T.D and Suarez, C.P
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 10/2020, Volume 56, Issue S1, pp. 187 - 187
Mosaicism | Trisomy | Ultrasonic imaging
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Somatic mosaicism for the COL7A1 mutation p.Gly2034Arg in the unaffected mother of a patient with dystrophic epidermolysis bullosa pruriginosa
by van den Akker, P. C and Pasmooij, A. M. G and Meijer, R and Scheffer, H and Jonkman, M. F
British journal of dermatology (1951), ISSN 1365-2133, 03/2015, Volume 172, Issue 3, pp. 778 - 781
GERMLINE MOSAICISM
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Mosaicism in Cutaneous Disorders
by Lim, Young H and Moscato, Zoe and Choate, Keith A
Annual review of genetics, ISSN 0066-4197, 11/2017, Volume 51, Issue 1, pp. 123 - 141
epigenetic mosaicism | lines of Blaschko | RASopathy | segmental mosaicism | nonsegmental mosaicism | somatic mutation | revertant mosaicism | Somatic mutation | Lines of Blaschko | Nonsegmental mosaicism | Epigenetic mosaicism | Segmental mosaicism | Revertant mosaicism | Embryo, Mammalian | Proto-Oncogene Proteins p21(ras) - genetics | Humans | Receptor, Fibroblast Growth Factor, Type 1 - metabolism | Keratin-10 - genetics | Laser Capture Microdissection | Keratin-1 - metabolism | Receptor, Fibroblast Growth Factor, Type 1 - genetics | Skin Diseases, Genetic - genetics | Ectoderm - pathology | Ectoderm - metabolism | Time Factors | Gene Expression Regulation, Developmental | Endoderm - pathology | Keratin-10 - metabolism | Proto-Oncogene Proteins p21(ras) - metabolism | Keratin-1 - genetics | Skin Diseases, Genetic - pathology | Skin Diseases, Genetic - metabolism | Endoderm - metabolism | Whole Exome Sequencing | Mosaicism | Mesoderm - metabolism | Mutation | Mesoderm - pathology | Cell differentiation | Research | Gametes | Pathogenesis | Therapeutic applications | Genomics | Genes | Disorders | Cells | Embryonic growth stage | Embryogenesis | Lesions | Pluripotency | Genotypes | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text EP04.30: Detection of fetal low rate of mosaicism Trisomy 8 by next‐generation sequencing of maternal plasma and invasive diagnosis
by Yan, K
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 10/2019, Volume 54, Issue S1, pp. 257 - 257
Mosaicism | Trisomy | Fetuses
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Paternal somatogonadal COL2A1 mosaicism causing recurrence of severe type 2 collagenopathy
by Morrison, Patrick J and Znaczko, Anna and Jansson, Mattias
American journal of medical genetics. Part A, ISSN 1552-4825, 09/2020, Volume 182, Issue 9, pp. 2191 - 2194
Mosaicism | Collagen | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text 2. CLINICAL COMPARISON OF TWO PGT-A PLATFORMS UTILIZING DIFFERENT THRESHOLDS TO DETERMINE PLOIDY STATUS
by Monahan, D and Harton, G and Griffin, D and Angle, M and Smikle, C
Reproductive biomedicine online, ISSN 1472-6483, 08/2019, Volume 39, pp. e27 - e28
aneuploidy | Mosaicism | PGT-A | NGS
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
11. Full Text 18. THE INSIGHTS OF EMBRYO MOSAICISM IN IVF CYCLES
by Coll, L and Parriego, M and Garcia-Monclús, S and Rodríguez, I and Boada, M and Coroleu, B and Vidal, F and Veiga, A
Reproductive biomedicine online, ISSN 1472-6483, 08/2019, Volume 39, pp. e25 - e26
biopsy | PGT-A | blastocyst | mosaicism
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
12. Full Text 31. CHROMOSOMAL MOSAICISM AS A RISK FACTOR FOR INCORRECT RESULTS OF PGT-A
by Kaimonov, V and Musatova, E and Khryapenkova, T and Zinina, J and Ilyin, K and Pomerantseva, E
Reproductive biomedicine online, ISSN 1472-6483, 08/2019, Volume 39, pp. e45 - e46
PGT-A | aCGH | mosaicism
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
13. Full Text Postzygotic single‐nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations
by Dou, Yanmei and Yang, Xiaoxu and Li, Ziyi and Wang, Sheng and Zhang, Zheng and Ye, Adam Yongxin and Yan, Linlin and Yang, Changhong and Wu, Qixi and Li, Jiarui and Zhao, Boxun and Huang, August Yue and Wei, Liping
Human mutation, ISSN 1059-7794, 08/2017, Volume 38, Issue 8, pp. 1002 - 1013
autistic traits | single‐nucleotide mosaicism | autism spectrum disorder | parental mosaicism | single-nucleotide mosaicism | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Autistic Disorder - genetics | Autism Spectrum Disorder - genetics | Genetic Predisposition to Disease - genetics | Humans | Male | Autistic Disorder - etiology | Exome - genetics | Alleles | Polymorphism, Single Nucleotide - genetics | Female | Mosaicism | Mutation | Autism Spectrum Disorder - etiology | Autism | Development and progression | Genetic aspects | Gene mutations | Analysis | Etiology | Single-nucleotide polymorphism | Children | Siblings | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights