Analysis of von Hippel-Lindau mutations with comparative genomic hybridization in sporadic and hereditary hemangioblastomas: Possible genetic heterogeneity

Biochemistry, Genetics and Molecular Biology

• Comparative Genomic Hybridization 100%
• Genetic Heterogeneity 100%
• Chromosome 3 100%
• Gene Mutation 50%
• Genetic Background 50%
• Carcinogenesis 50%
• Tumor Suppressor Gene 50%
• Chromosomal Aberration 50%
• Protein Function 50%
• Von Hippel-Lindau Disease 50%
• Chromosome 3p 50%
• Von Hippel-Lindau Tumor Suppressor 50%

Keyphrases

• Genetic Heterogeneity 100%
• Comparative Genomic Hybridization 100%
• Von Hippel-Lindau Disease 100%
• Hemangioblastoma 100%
• Von Hippel-Lindau 33%
• Chromosomal Abnormalities 16%
• Tumor 11%
• Chromosome 3 11%
• Genetic Background 5%
• Molecular Mechanism 5%
• Tumor Suppressor Gene 5%
• Tumorigenesis 5%
• Chromosomal Aberrations 5%
• Protein Function 5%
• Gene mutation 5%
• Mutation Analysis 5%
• Clinical Criteria 5%
• Direct Sequencing 5%
• Chromosome 3p 5%
• Von Hippel-Lindau Tumor Suppressor 5%
• Inhibition Mechanism 5%
• Protein Inactivation 5%