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

Search Articles

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (225) 225
science & technology (214) 214
life sciences & biomedicine (208) 208
genetics & heredity (143) 143
mutation (129) 129
male (128) 128
life sciences (116) 116
female (97) 97
genetics (79) 79
biological and medical sciences (78) 78
medical sciences (73) 73
adult (65) 65
cystic fibrosis (64) 64
cystic fibrosis - genetics (58) 58
cystic fibrosis transmembrane conductance regulator - genetics (57) 57
biochemistry & molecular biology (51) 51
dna mutational analysis (47) 47
child (45) 45
[sdv]life sciences [q-bio] (44) 44
genes (39) 39
phenotype (38) 38
adolescent (37) 37
base sequence (37) 37
molecular sequence data (37) 37
alleles (35) 35
genotype (34) 34
pedigree (34) 34
exons (33) 33
genetic aspects (33) 33
human genetics (32) 32
medical genetics (31) 31
haplotypes (29) 29
polymerase chain reaction (29) 29
[sdv.gen]life sciences [q-bio]/genetics (28) 28
dystrophin - genetics (27) 27
middle aged (27) 27
cystic fibrosis transmembrane conductance regulator (25) 25
fundamental and applied biological sciences. psychology (25) 25
child, preschool (24) 24
polymorphism, genetic (24) 24
genetics of eukaryotes. biological and molecular evolution (22) 22
mutation - genetics (22) 22
research (22) 22
[sdv.gen.gh]life sciences [q-bio]/genetics/human genetics (21) 21
human health and pathology (21) 21
biochemistry, molecular biology (20) 20
point mutation (20) 20
france (19) 19
genetic variation (19) 19
infant, newborn (19) 19
analysis (18) 18
gene expression (18) 18
molecular and cellular biology (18) 18
sequence deletion (18) 18
congenital, hereditary, and neonatal diseases and abnormalities (17) 17
gene mutations (17) 17
general aspects. genetic counseling (17) 17
heterozygote (17) 17
muscular dystrophy, duchenne - genetics (17) 17
dystrophin (16) 16
exons - genetics (16) 16
gene frequency (16) 16
neurology (16) 16
usher syndromes - genetics (16) 16
young adult (16) 16
cftr (15) 15
man (15) 15
marfan syndrome (15) 15
membrane proteins - genetics (15) 15
mesh: humans (15) 15
clinical neurology (14) 14
databases, genetic (14) 14
diagnosis (14) 14
frameshift mutation (14) 14
gastroenterology. liver. pancreas. abdomen (14) 14
genomics (14) 14
introns (14) 14
liver. biliary tract. portal circulation. exocrine pancreas (14) 14
neurosciences & neurology (14) 14
other diseases. semiology (14) 14
vas deferens - abnormalities (14) 14
alternative splicing (13) 13
cystic fibrosis - diagnosis (13) 13
extracellular matrix proteins - genetics (13) 13
fibrillin-1 (13) 13
fibrillins (13) 13
genetic disorders (13) 13
marfan syndrome - genetics (13) 13
microfilament proteins - genetics (13) 13
molecular biology (13) 13
musculoskeletal diseases (13) 13
ophthalmology (13) 13
[sdv.bbm.bm]life sciences [q-bio]/biochemistry, molecular biology/molecular biology (12) 12
bioinformatics (12) 12
deoxyribonucleic acid--dna (12) 12
dna - genetics (12) 12
duchenne muscular dystrophy (12) 12
infant (12) 12
otorhinolaryngologic diseases (12) 12
pregnancy (12) 12
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Human mutation, ISSN 1059-7794, 03/2015, Volume 36, Issue 3, pp. v - v
Journal Article
Journal Article
European journal of human genetics : EJHG, ISSN 1018-4813, 07/2015, Volume 23, Issue 7, pp. 929 - 934
Journal Article