Medicine and Dentistry
Gene
54%
Patient
38%
Protein
34%
Epidermolysis bullosa
33%
Disease
29%
Skin Fragility
26%
Syndrome
24%
Family
21%
Poikiloderma
20%
Prenatal Diagnosis
16%
Analysis
15%
Epidermolytic Hyperkeratosis
15%
Keratin 1
13%
DNA
12%
Cells
12%
Skin Biopsy
11%
Hair
11%
Genodermatosis
11%
Dermatosis
10%
Ectodermal Dysplasia
10%
Desmoglein 1
9%
Keratin
9%
Man
9%
Epidermolysis Bullosa Dystrophica
9%
Differentiation
9%
EEC Syndrome
8%
Autosomal Recessive Inheritance
8%
Esophageal Stricture
8%
Keratoderma
8%
Squamous Cell Carcinoma
8%
Amino Terminal Sequence
7%
Mutant
6%
Gap Junction
6%
Epidermolytic Palmoplantar Keratoderma
6%
Chorionic Villus Sampling
6%
Sense
6%
Psoriasis
6%
Hair Follicle
6%
Experience
6%
Paramethasone
6%
Pyloric Atresia
6%
Epidermolysis Bullosa Simplex
6%
Photosensitivity Disorder
6%
Filaggrin
6%
Therapeutics
6%
Erythrokeratodermia variabilis
6%
Genomic Organization
6%
Keratin 15
6%
Keratin 19
6%
Heterozygosity
6%
Biochemistry, Genetics and Molecular Biology
Gene
100%
Protein
68%
Epidermolysis bullosa
51%
Exon
35%
Dysplasia
31%
Desmoglein-1
19%
Sequencing
18%
Genomics
16%
Genodermatosis
15%
Preimplantation Genetic Diagnosis
14%
Amino Acids
11%
Autosomal Recessive Disorder
10%
Frameshift Mutation
8%
N-Terminus
7%
Gene Linkage
7%
DSC1
6%
Desmoglein-3
6%
Compound Heterozygosity
6%
Insulin-Like Growth Factor-Binding Protein
6%
Stem Cell
6%
Case Report
6%
Spectrum
6%
Isoform
6%
Extracellular Matrix Protein
6%
Granulation Tissue
6%
Membrane
6%
Cytoskeleton
6%
Genetic Linkage
5%
