Biochemistry, Genetics and Molecular Biology
Genetics
66%
Retinitis pigmentosa
44%
Genetic Counseling
44%
Genetic Heterogeneity
33%
Clinical Study
33%
Clinical Trial
33%
Gene Polymorphism
33%
Contig
33%
Lymphocyte
33%
Cosmid
22%
Exon Trapping
16%
Chromosome 11p
16%
Restriction Enzyme
11%
Gene Linkage Disequilibrium
11%
Chromosome 11q
11%
Tissue Distribution
11%
Mental Stress
11%
Shotgun Sequencing
11%
Conserved Sequence
11%
Chromosome 14q
11%
Computer Analysis
11%
DNA Sequence
11%
CpG Island
11%
Isoform
11%
Keyphrases
Collaborative Study
83%
Usher Syndrome
83%
Genetic Studies
14%
Sweden
14%
Genetic Counseling
10%
Retinitis pigmentosa
10%
Etiology
10%
Pigmentosa
9%
Expressed Sequence
7%
Congenital Deafness
7%
Clinical Variation
7%
Affected Siblings
7%
Vestibular Disorders
7%
Underlying Etiologies
7%
Clinical Evaluation
7%
Lymphocytes
7%
Audiology
7%
Vestibular
7%
Genetic Heterogeneity
7%
DNA Polymorphism
7%
Distinct Subtypes
7%
Profound Deafness
7%
Genetic Treatment
7%
Congenital Hearing Loss
7%
Congenitally Deaf
7%
As(V)
7%
Ophthalmological
7%
Most Common Form
7%
Chromosome 11p
5%
Exon Trapping
5%
Medicine and Dentistry
Usher Syndrome
100%
Disease
19%
Congenital Hearing Loss
16%
Genetic Counseling
13%
Retinitis pigmentosa
13%
Contig
11%
DNA Polymorphism
9%
Clinical Trial
9%
Hearing Impairment
9%
Genetic Heterogeneity
9%
Clinical Study
9%
Lymphocyte
9%
Vestibular Disorder
9%
Cosmid
7%
Conserved Sequence
5%
Computer Analysis
5%
Chromosome 11p
5%