Keyphrases
MSH2
100%
MSH6
100%
Intronic mutation
100%
MLH1
100%
Colorectal Cancer Patients
100%
Functional Assessment
100%
MSH2 Gene
18%
Intronic Variant
18%
In Silico Prediction Tools
18%
Minigene Assay
18%
MSH6 Gene
18%
Aberrant Splicing
9%
Colorectal Cancer
9%
Frameshift mutation
9%
In Silico
9%
Variants of Uncertain Significance
9%
Splicing mutation
9%
Genetic Counseling
9%
Family Members
9%
Study Support
9%
Germline mutation
9%
DNA Mismatch Repair Genes
9%
Lynch Syndrome
9%
Missense Variants
9%
Hereditary Colorectal Cancer Syndromes
9%
Nonsense mutation
9%
Complex Chromosomal Rearrangement
9%
In Vitro Characterization
9%
Silent Variant
9%
Cause of Disease
9%
Biochemistry, Genetics and Molecular Biology
MSH6
100%
MLH1
100%
MSH2
100%
Minigene
18%
Genetic Counseling
9%
Germline Mutation
9%
Missense
9%
Genomics
9%
Wild Type
9%
DNA Mismatch Repair
9%