X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (210) 210
Publication (75) 75
Patent (39) 39
Conference Proceeding (21) 21
Book / eBook (14) 14
Dissertation (6) 6
Book Review (3) 3
Book Chapter (2) 2
Music Score (2) 2
Magazine Article (1) 1
Streaming Audio (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (92) 92
index medicus (85) 85
mutation (62) 62
female (61) 61
genetics & heredity (61) 61
male (60) 60
life sciences (57) 57
physics (44) 44
calculating (38) 38
computing (38) 38
counting (38) 38
electric digital data processing (38) 38
genetics (38) 38
adult (30) 30
genetic aspects (29) 29
child (26) 26
phenotype (25) 25
adolescent (23) 23
animals (22) 22
electric communication technique (22) 22
electricity (22) 22
mutations (22) 22
child, preschool (21) 21
human health and pathology (21) 21
research (21) 21
gene (19) 19
optics (19) 19
optical elements, systems, or apparatus (18) 18
[ sdv.mhep ] life sciences [q-bio]/human health and pathology (17) 17
article (17) 17
human genetics (17) 17
image data processing or generation, in general (17) 17
pedigree (17) 17
genes (16) 16
intellectual disability (16) 16
biochemistry & molecular biology (15) 15
genetic predisposition to disease (15) 15
infant (15) 15
young adult (15) 15
advertising (14) 14
arrangements or circuits for control of indicating devicesusing static means to present variable information (14) 14
cryptography (14) 14
display (14) 14
education (14) 14
proteins (14) 14
seals (14) 14
disease (13) 13
gene mutations (13) 13
infant, newborn (13) 13
intellectual disability - genetics (13) 13
mice (13) 13
clinical neurology (12) 12
data processing systems or methods, specially adapted foradministrative, commercial, financial, managerial, supervisoryor forecasting purposes (12) 12
genetic disorders (12) 12
pictorial communication, e.g. television (12) 12
systems or methods specially adapted for administrative,commercial, financial, managerial, supervisory or forecastingpurposes, not otherwise provided for (12) 12
transmission of digital information, e.g. telegraphiccommunication (12) 12
analysis (11) 11
diagnosis (11) 11
family (11) 11
genotype (11) 11
genotype & phenotype (11) 11
health aspects (11) 11
middle aged (11) 11
neurosciences (11) 11
patients (11) 11
syndrome (11) 11
exome - genetics (10) 10
genetic variation (10) 10
genomes (10) 10
human necessities (10) 10
molecular sequence data (10) 10
[ sdv.gen.gh ] life sciences [q-bio]/genetics/human genetics (9) 9
abnormalities, multiple - genetics (9) 9
cancer (9) 9
expression (9) 9
genetic predisposition to disease - genetics (9) 9
genomics (9) 9
identification (9) 9
intellectual disabilities (9) 9
phenotypes (9) 9
physiological aspects (9) 9
protein (9) 9
sequence analysis, dna (9) 9
zebrafish (9) 9
[ sdv.gen ] life sciences [q-bio]/genetics (8) 8
aged (8) 8
alleles (8) 8
cabinets (8) 8
coffee mills (8) 8
desks (8) 8
domestic articles or appliances (8) 8
drawers (8) 8
epilepsy (8) 8
exome sequencing (8) 8
furniture (8) 8
general details of furniture (8) 8
genetic testing (8) 8
medical research (8) 8
mosaicism (8) 8
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (7) 7
UTL at Downsview - May be requested (4) 4
Online Resources - Online (2) 2
Thomas Fisher Rare Book - Rare Book (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Music - Stacks (1) 1
Robarts - May be requested in 6-10 wks (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
Trinity College (John W Graham) - Strachan (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Brain, ISSN 0006-8950, 06/2015, Volume 138, Issue 6, pp. 1613 - 1628
Journal Article
Genetics in medicine : official journal of the American College of Medical Genetics, ISSN 1098-3600, 08/2019
Our laboratory has classified patients with methylmalonic aciduria using somatic cell studies for over four decades. We have accumulated 127 fibroblast lines... 
Journal Article
Nature Genetics, ISSN 1061-4036, 08/2012, Volume 44, Issue 8, pp. 934 - 940
Journal Article
Pediatric dermatology, ISSN 0736-8046, 07/2019
Cutaneous patterned hypopigmentation's phenotype is highly variable and may be associated with extracutaneous anomalies. We evaluated the phenotypic and... 
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 10/2019, p. 88307381987891
The term spinocerebellar ataxia encompasses a heterogeneous group of neurodegenerative disorders due to pathogenic variants in more than 100 genes, underlying... 
Journal Article
Th.--Méd.--Paris, 1830. Voyez tome 6, page N ° 193. Paris, 1830. 
Dissertation
Th.--Méd.--Paris, 1840. Voyez tome 15, page N ° 234. Paris, 1840. 
Dissertation
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, ISSN 1058-4838, 02/2019
Mycobacterium canettii forms part of the Mycobacterium tuberculosis complex. M. canettii infections are mainly described in the Horn of Africa. The permanent... 
Journal Article
Journal of Investigative Dermatology, ISSN 0022-202X, 04/2016, Volume 136, Issue 4, pp. 770 - 778
Journal Article
Clinical Genetics, ISSN 0009-9163, 06/2016, Volume 89, Issue 6, pp. 700 - 707
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2018, Volume 1865, pp. 233 - 241
Accessibility and imaging of cell compartments in big specimens are crucial for cellular biological research but also a matter of contention. Confocal imaging... 
Tissue clearing | Fructose-based high-refractive index solution | 3D imaging | Brain - metabolism | Head | Animals | Xenopus laevis - embryology | Larva | Xenopus laevis - metabolism | Imaging, Three-Dimensional - methods | Fluorescent Dyes - metabolism | Pigmentation | Triiodothyronine - pharmacology
Journal Article
European Journal of Preventive Cardiology, ISSN 2047-4873, 8/2019, Volume 26, Issue 12, pp. 1262 - 1270
Aims Familial hypercholesterolemia (FH) is the most common genetic disorder in medicine, with a prevalence of 1/250. Affected individuals have elevated... 
atherosclerotic cardiovascular disease | Familial hypercholesterolemia | genetic testing | low-density lipoprotein | PANEL | CARDIAC & CARDIOVASCULAR SYSTEMS | SOCIETY POSITION STATEMENT | CLINICIAN | GUIDANCE | LDL CHOLESTEROL | DISEASE | RECEPTOR GENE | MUTATIONS | INSIGHTS
Journal Article
Arthritis Care and Research, ISSN 2151-464X, 09/2017, Volume 69, Issue 9, pp. 1429 - 1436
Journal Article