X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (136) 136
male (89) 89
female (86) 86
genetics & heredity (61) 61
index medicus (50) 50
pedigree (50) 50
adult (45) 45
mutation (33) 33
denmark (32) 32
genetic linkage (30) 30
middle aged (30) 30
phenotype (25) 25
gene (24) 24
biochemistry & molecular biology (23) 23
child (23) 23
chromosome mapping (22) 22
genotype (21) 21
alleles (20) 20
genetic aspects (20) 20
base sequence (19) 19
genetics (19) 19
molecular sequence data (19) 19
adolescent (17) 17
expression (16) 16
linkage (16) 16
lod score (16) 16
dna mutational analysis (15) 15
gene frequency (15) 15
research (15) 15
aged (14) 14
endocrinology & metabolism (14) 14
locus (14) 14
polymorphism, genetic (14) 14
amino acid sequence (13) 13
family (13) 13
haplotypes (13) 13
child, preschool (12) 12
genes, dominant (12) 12
genetic markers (12) 12
linkage analysis (12) 12
mutations (12) 12
polymerase chain reaction (12) 12
type 2 diabetes (12) 12
genes (11) 11
risk (11) 11
risk factors (11) 11
sequence analysis, dna (11) 11
animals (10) 10
association (10) 10
cataract - genetics (10) 10
diabetes mellitus, type 2 - genetics (10) 10
disease (10) 10
polymorphism, single nucleotide (10) 10
analysis (9) 9
case-control studies (9) 9
denmark - epidemiology (9) 9
genetic variation (9) 9
internal medicine (9) 9
obesity (9) 9
population (9) 9
chromosomes (8) 8
diabetes (8) 8
glucose (8) 8
health aspects (8) 8
loci (8) 8
multidisciplinary sciences (8) 8
physiological aspects (8) 8
prevalence (8) 8
research article (8) 8
cohort studies (7) 7
diabetes mellitus, type 2 - blood (7) 7
dna (7) 7
dna primers (7) 7
exons (7) 7
genomes (7) 7
haplotypes - genetics (7) 7
human genetics (7) 7
identification (7) 7
infant (7) 7
infant, newborn (7) 7
insulin (7) 7
medicine (7) 7
mutation - genetics (7) 7
mutation, missense (7) 7
neurosciences (7) 7
ophthalmology (7) 7
polymorphism (7) 7
proteins (7) 7
body mass index (6) 6
cataract - congenital (6) 6
clinical neurology (6) 6
european continental ancestry group - genetics (6) 6
family health (6) 6
genetic predisposition to disease (6) 6
genomics (6) 6
glucose tolerance test (6) 6
greenland (6) 6
heterozygote (6) 6
human genome (6) 6
inuits - genetics (6) 6
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Genetics, ISSN 1061-4036, 2006, Volume 38, Issue 6, pp. 668 - 673
Journal Article
Journal Article
Nature, ISSN 0028-0836, 08/2017, Volume 548, Issue 7665, pp. 87 - 91
Journal Article
European Respiratory Journal, ISSN 0903-1936, 08/2017, Volume 50, Issue 2, pp. 1700423 - 1700423
Respiratory symptoms on exertion, such as shortness of breath and wheezing, are commonly associated with asthma, but might also arise from the larynx [1–3]. In... 
RESPIRATORY SYSTEM | CONGENITAL LARYNGOMALACIA | PREVALENCE | Inheritance Patterns | Airway Obstruction - complications | Exercise | Airway Obstruction - genetics | Cross-Sectional Studies | Dyspnea - genetics | Humans | Sex Factors | Family | Female | Male | Dyspnea - etiology | Adolescence | Child development | Sex differences | Wheezing | Larynx | Respiration | Laryngoscopy | Asthma
Journal Article
Journal Article
Journal Article
Journal Article
Journal Article
MOLECULAR VISION, ISSN 1090-0535, 01/2019, Volume 25, Issue 1, pp. 1 - 11
Purpose: To identify the mutation for Volkmann cataract (CTRCT8) at 1p36.33. Methods: The genes in the candidate region 1p36.33 were Sanger and parallel deep... 
MESSENGER-RNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | OPHTHALMOLOGY | DOMINANT CONGENITAL CATARACT | MICRORNAS | MUTATIONS | EPITHELIAL-CELL APOPTOSIS | CONTAINS | EXPRESSION | LAMELLAR | LOCUS | AGE | cataract
Journal Article