Germline PTEN mutations in Cowden syndrome-like families

Medicine and Dentistry

• Cowden Syndrome 100%
• Family 53%
• Diagnosis 13%
• Breast 13%
• Patient 13%
• Tensin 6%
• Phenotype 6%
• Protein P53 6%
• Sequence Analysis 6%
• Missense Mutation 6%
• Breast Carcinoma 6%
• Tumor Suppressor Gene 6%
• Ovarian Cancer 6%
• Nucleotide 6%
• Gel Electrophoresis 6%
• BRCA1 6%
• BRCA2 6%
• Thyroid Carcinoma 6%
• Point Mutation 6%
• Autosomal Dominant Disorder 6%
• Exon 6%
• Germline Mutation 6%
• Frameshift Mutation 6%
• Nonsense Mutation 6%
• Pathognomonic 6%
• Dual Specificity Phosphatase 6%
• Cytoskeleton Protein 6%
• Gene 6%
• Thyroid Follicular Carcinoma 6%
• Denaturing Gradient Gel Electrophoresis 6%
• Auxilin 6%
• Male 6%

Biochemistry, Genetics and Molecular Biology

• Germline 26%
• Mutation 20%
• Gel Electrophoresis 13%
• Tumor Suppressor Protein 13%
• Tensin 6%
• Nested Gene 6%
• Nucleotide 6%
• Phenotype 6%
• P53 6%
• Exon 6%
• Protein Sequencing 6%
• Germline Mutation 6%
• BRCA2 6%
• Point Mutation 6%
• Autosomal Dominant Inheritance 6%
• Missense Mutation 6%
• BRCA1 6%
• Nonsense Mutation 6%
• Auxilin 6%
• Temperature 6%
• Frameshift Mutation 6%
• Dual-Specificity Phosphatase 6%
• Cytoskeletal Protein 6%