Medicine & Life Sciences
Mutation
100%
Fuchs' Endothelial Dystrophy
93%
Cataract
69%
Lenses
59%
Chromosomes
59%
Retinal Degeneration
52%
Genome
40%
Exons
40%
Microsatellite Repeats
38%
Phenotype
35%
Missense Mutation
34%
Genes
33%
Eye
29%
Pedigree
28%
Retinal Dystrophies
24%
Haplotypes
23%
DNA
23%
Exome
23%
Corneal Endothelium
22%
Lod Score
21%
Autophagy
20%
Glaucoma
20%
Proteins
19%
Alleles
19%
Descemet Membrane
19%
Induced Pluripotent Stem Cells
18%
Congenital stationary night blindness
17%
Proteome
16%
Human Embryonic Stem Cells
16%
Cornea
15%
Crystalline Lens
14%
Whole Exome Sequencing
14%
Endothelial Cells
14%
Pakistan
14%
Photography
14%
Night Blindness
13%
Corneal Transplantation
12%
Type 6 Cyclic Nucleotide Phosphodiesterases
12%
Retina
12%
Gene Expression Profiling
11%
Introns
11%
Stem Cells
10%
Nonsyndromic Deafness
10%
Electroretinography
10%
Autosomal Recessive 63 Deafness
10%
Hearing Loss
10%
Crystallins
10%
Corneal Dystrophy, Fuchs Endothelial, 2
10%
Population
9%