about
P1889
POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillanceNew insights into POLE and POLD1 germline mutations in familial colorectal cancer and polyposisMLH1 promoter hypermethylation in the analytical algorithm of Lynch syndrome: a cost-effectiveness study.Detection of genetic alterations in hereditary colorectal cancer screening.Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study.Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype.Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis.Prevalence of germline MUTYH mutations among Lynch-like syndrome patients.High risk of endometrial cancer in colorectal cancer kindred is pathognomonic for MMR-mutation carriers.K-ras and p16 aberrations confer poor prognosis in human colorectal cancerNon-Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in theMSH2 gene
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Sara González
@ast
Sara González
@en
Sara González
@es
Sara González
@nl
type
label
Sara González
@ast
Sara González
@en
Sara González
@es
Sara González
@nl
prefLabel
Sara González
@ast
Sara González
@en
Sara González
@es
Sara González
@nl
P1053
D-8427-2019
P106
P1889
P21
P31
P496
0000-0002-7765-1325