X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Newspaper Article (44) 44
Journal Article (33) 33
Book / eBook (8) 8
Publication (6) 6
Book Review (4) 4
Book Chapter (1) 1
Dissertation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (20) 20
humans (15) 15
female (11) 11
genetics & heredity (7) 7
male (7) 7
mutation (7) 7
disease (6) 6
prime ministers (6) 6
adult (5) 5
animals (5) 5
genetics (5) 5
medicine (5) 5
amino acid sequence (4) 4
cancer (4) 4
middle aged (4) 4
pedigree (4) 4
phenotype (4) 4
analysis (3) 3
automobile drivers (3) 3
bodembescherming (3) 3
bodenerosion (3) 3
bodenschutz (3) 3
child, preschool (3) 3
clinical neurology (3) 3
commercial real estate (3) 3
conservation (3) 3
education (3) 3
gene (3) 3
genetic aspects (3) 3
genetic disorders (3) 3
genomics (3) 3
genotype & phenotype (3) 3
leadership (3) 3
mass spectrometry (3) 3
metabolomics - methods (3) 3
molecular sequence data (3) 3
neurosciences (3) 3
population (3) 3
prevention (3) 3
research (3) 3
soil conservation (3) 3
sols (3) 3
students (3) 3
traffic congestion (3) 3
acid (2) 2
aged (2) 2
alpha-tropomyosin (2) 2
arthrogryposis (2) 2
arthrogryposis - genetics (2) 2
attitudes (2) 2
biochemistry & molecular biology (2) 2
biomarkers (2) 2
biomarkers - blood (2) 2
biopsy (2) 2
bodemerosie (2) 2
breast neoplasms - etiology (2) 2
caloric restriction (2) 2
careers (2) 2
central business districts (2) 2
chemometrics (2) 2
chief executive officers (2) 2
child (2) 2
chromatography (2) 2
committees (2) 2
congenital diseases (2) 2
conservación de suelos (2) 2
decision making (2) 2
erosión (2) 2
exome - genetics (2) 2
expression (2) 2
family medical history (2) 2
fiber-type disproportion (2) 2
gas chromatography-mass spectrometry (2) 2
gas-chromatography (2) 2
gene expression (2) 2
genetic counseling (2) 2
health aspects (2) 2
housing (2) 2
immunology (2) 2
inequality (2) 2
infant (2) 2
knowledge (2) 2
light rail transportation (2) 2
lipids - blood (2) 2
magnetic resonance spectroscopy (2) 2
medical research (2) 2
metabolism (2) 2
methods (2) 2
microbiology (2) 2
muscular diseases - genetics (2) 2
mutation - genetics (2) 2
mutations (2) 2
nemaline myopathy (2) 2
oncology (2) 2
parliaments (2) 2
pathogenesis (2) 2
proteins (2) 2
public health (2) 2
report (2) 2
reproductive medicine (2) 2
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (3) 3
UofT at Mississauga - Stacks (2) 2
Institute for Christian Studies - Stacks (1) 1
Pontifical Inst. Mediaeval Studies - Library use only (1) 1
Robarts - Stacks (1) 1
Thomas Fisher Rare Book - Rare Book (1) 1
Trinity College (John W Graham) - Rare Book (1) 1
UTL at Downsview - May be requested (1) 1
UofT at Scarborough - Stacks (1) 1
Victoria University E.J. Pratt - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 09/2014, Volume 85, Issue 9, pp. 1058 - 1060
  To identify the molecular cause of the disease, either in one of the eight known nemaline myopathy genes not yet sequenced in the proband, or in a novel gene... 
SURGERY | DISRUPTION | GENE | PSYCHIATRY | CLINICAL NEUROLOGY | MUTATION | Base Sequence - genetics | Genetic Predisposition to Disease - genetics | Myopathies, Nemaline - genetics | Pedigree | Humans | Adult | Female | Infant | Male | Cofilin 2 - genetics | Sequence Deletion - genetics | Proteins | Disease | Biopsy | Genes | Ventilation | Mutation | Deoxyribonucleic acid--DNA | Index Medicus
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 11/2015, Volume 10, Issue 1, pp. 148 - 148
Journal Article
BMJ Open, ISSN 2044-6055, 06/2019, Volume 9, Issue 6, pp. e028209 - e028209
IntroductionPreconception carrier screening (PCS) identifies couples at risk of having children with recessive genetic conditions. New technologies have... 
pilot study protocol | reproductive medicine | genetic carrier screening | attitudes | knowledge | Medicine | Medical research | Genetic counseling | Disease | Laboratories | Genomics | Population | Genetics | Family medical history | Cost analysis | Public health
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 12/2018, Volume 27, Issue 24, pp. 4263 - 4272
Abstract Congenital myopathies are typically characterised by early onset hypotonia, weakness and hallmark features on biopsy. Despite the rapid pace of gene... 
ESSENTIAL LIGHT-CHAIN | FIBER-TYPE DISPROPORTION | OVEREXPRESSION | HYPERTROPHY | MYOSIN | GENETICS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISEASE | GENETICS & HEREDITY | COMMON-CAUSE | Index Medicus
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 03/2018, Volume 102, Issue 3, pp. 505 - 514
Journal Article