Keyphrases
Congenital Cataract
90%
Eye Color
67%
Founder mutation
67%
HERC2
67%
Mutational Screening
67%
Long Non-coding RNA (LncRNA)
67%
Cataract
67%
Splice Variant
67%
Quantitative PCR
45%
Non-coding RNA (ncRNA)
45%
Linkage Analysis
45%
Linkage Region
45%
Sanger
45%
Mammalian Genome
22%
RNA-binding Protein
22%
MicroRNA
22%
New Markers
22%
Deep Resequencing
22%
Crosslinking Immunoprecipitation
22%
Histone Methylation
22%
Sanger Sequencing
22%
Single nucleotide Polymorphism
22%
Exon
22%
GNB1
22%
Expression Analysis
22%
Deep Sequencing
22%
Healthy Individuals
22%
Splice Site
22%
Polymerase Chain Reaction Analysis
22%
Primates
22%
Histone Acetylation
22%
Transcription Factor Binding Sites
22%
Sequence Data
22%
Autosomal Dominant
22%
Bioinformatics Analysis
22%
Regulatory Function
22%
Donor Splice Site
22%
Marker System
22%
Genomic Regions
22%
Meta-analysis
22%
Alternative Transcripts
22%
Intron Splicing
22%
Human Tissue
22%
Microcornea
16%
CRYBB2
16%
Identification Rate
16%
Causal mutation
16%
Mutation Identification
16%
HSF4
16%
Hereditary Eye Diseases
16%
Biochemistry, Genetics and Molecular Biology
Linkage Analysis
100%
OCA2
67%
HERC2
67%
Eye Color
67%
Long Non-Coding RNA
67%
Regulatory Element
67%
Allele
53%
Transcription Factor
45%
Gene Conversion
33%
Connexin
33%
Genotype Phenotype Correlation
33%
Candidate Gene
32%
Gene Linkage
22%
Reverse Transcription Polymerase Chain Reaction
22%
Intron
20%
Promoter Region
19%
Hair Color
19%
Single Nucleotide Polymorphism
19%
