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Risk of new tumors in von Hippel-Lindau patients depends on age and genotype
Marie Louise Mølgaard Binderup,
Esben Budtz-Jørgensen
,
Søs Marie Luise Bisgaard
Medical Genetics Program
Biostatistisk afdeling
8
Citationer (Scopus)
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Keyphrases
Genotype
100%
New Tumor
100%
Von Hippel-Lindau
100%
Mutation Carriers
75%
VHL Gene
50%
Tumor Development
50%
Teenage Years
50%
Tumor Genotyping
25%
Missense mutation
25%
Tumor Location
25%
Retinal Tumor
25%
Genomic Surveillance
25%
Genetic Counseling
25%
Adulthood
25%
Poisson Regression
25%
Hazard Ratio
25%
Confidence Interval
25%
Anatomical Location
25%
Cerebellar Tumor
25%
Tumor Site
25%
National Cohort Study
25%
Biochemistry, Genetics and Molecular Biology
Genotyping
100%
Adolescence
66%
Lifespan
66%
Genetic Counseling
33%
Missense Mutation
33%
Cohort Study
33%
Medicine and Dentistry
Neoplasm
100%
Lifespan
33%
Adolescence
33%
Study Subject
16%
Hazard Ratio
16%
Missense Mutation
16%
Genetic Counseling
16%
Cerebellum Tumor
16%
Retina Tumor
16%
Cohort Analysis
16%
Immunology and Microbiology
Lifespan
100%
Adolescence
100%
Missense Mutation
50%
Pharmacology, Toxicology and Pharmaceutical Science
Neoplasm
100%
Cerebellum Tumor
16%
Cohort Study
16%
Retina Tumor
16%
Neuroscience
Missense Mutation
100%