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Publications by Amelia Casamassimi
APC and MUTYH Analysis in FAP Patients: A Novel Mutation in APC Gene and Genotype-Phenotype Correlation
Genes
Genetics
Hypoxia-Regulated miRNAs in Human Mesenchymal Stem Cells: Exploring the Regulatory Effects in Ischemic Disorders
International Journal of Molecular Sciences
Organic Chemistry
Molecular Biology
Theoretical Chemistry
Inorganic Chemistry
Computer Science Applications
Spectroscopy
Medicine
Catalysis
Physical
Related publications
A Novel Aberrant Splice Site Mutation in the APC Gene
Journal of Medical Genetics
Genetics
Can APC Mutation Analysis Contribute to Therapeutic Decisions in Familial Adenomatous Polyposis? Experience From 680 FAP Families
Gut
Gastroenterology
Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome
American Journal of Human Genetics
Genetics
Phenotype/Genotype Correlation in a Case Series of Stargardt’s Patients Identifies Novel Mutations in the ABCA4 Gene
Eye
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
Correlation Between the Methylation of APC Gene Promoter and Colon Cancer
Oncology Letters
Cancer Research
Oncology
APC Mutation and Phenotypic Spectrum of Singapore Familial Adenomatous Polyposis Patients
European Journal of Human Genetics
Genetics
Aggressive Gastric Cancer in a Patient With an APC Mutation and a Monoallelic MYH Mutation
Hereditary Cancer in Clinical Practice
Oncology
Genetics
Racial Variation in Frequency and Phenotypes of APC and MUTYH Mutations in 6,169 Individuals Undergoing Genetic Testing
Genetics in Medicine
Medicine
Genetics
Genotype and Phenotype in Patients With Noonan Syndrome and a RIT1 Mutation
Genetics in Medicine
Medicine
Genetics