Analysis of the PTCH coding region in human rhabdomyosarcoma

Keyphrases

• Coding Region 100%
• Rhabdomyosarcoma 100%
• Tumor 40%
• Protein-coding Genes 40%
• Polymorphism 40%
• Nevoid Basal Cell Carcinoma Syndrome 40%
• Missense mutation 20%
• Nonsense mutation 20%
• Autosomal Dominant Disorder 20%
• Exon 20%
• Tumor Suppressor Gene 20%
• Fibroma 20%
• Tumor Formation 20%
• Human Tumors 20%
• Medulloblastoma 20%
• Basal Cell Carcinoma 20%
• Developmental Abnormality 20%
• Frequent mutation 20%
• Human Case 20%
• Ptch 20%
• Inherited mutation 20%

Neuroscience

• Coding Region 100%
• Autosomal Dominant Disorder 20%
• Nonsense Mutation 20%
• Missense Mutation 20%
• Tumor Suppressor Gene 20%
• Exon 20%
• Carcinogenesis 20%
• Medulloblastoma 20%
• Inherited Mutation 20%

Biochemistry, Genetics and Molecular Biology

• Coding Region 100%
• Exon 20%
• Tumor Suppressor Gene 20%
• Autosomal Dominant Inheritance 20%
• Missense Mutation 20%
• Nonsense Mutation 20%
• Carcinogenesis 20%
• Inherited Mutation 20%