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Novel genetic mutations detected by multigene panel are associated with hereditary colorectal cancer predispositionDoes multilocus inherited neoplasia alleles syndrome have severe clinical expression?Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer PatientsLarge scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
P50
description
researcher (ORCID 0000-0001-6045-7879)
@en
wetenschapper
@nl
name
Paula Rofes
@en
Paula Rofes
@nl
type
label
Paula Rofes
@en
Paula Rofes
@nl
prefLabel
Paula Rofes
@en
Paula Rofes
@nl
P31
P496
0000-0001-6045-7879