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A38BRCA1/2 mutations and hereditary breast cancer: clinical phenotype, type of mutation and founder effect
A38BRCA1/2 mutations and hereditary breast cancer: clinical phenotype, type of mutation and founder effect
2015
Z. Ballatore
R. Bracci
Mirco Pistelli
F. Bianchi
Elena Maccaroni
L. Belvederesi
V. Panni
M. De Lisa
A. Della Mora
A. Pagliacci
Nicola Battelli
Alfredo Santinelli
Tommasina Biscotti
Stefano Cascinu
Keywords:
Hereditary Breast Cancer
Pathology
Phenotype
Medicine
Familial breast cancer
Cancer research
Founder effect
Mutation
clinical phenotype
brca1 protein
Correction
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