Molecular tumour pathology - and tumour geneticsMTG2 - Moleculaire genetica van gastrointestinale tumore
Colorectal cancer is one of the most frequent neoplasms and an important cause of mortality in the d...
The present article summarizes recent developments in the characterization of genetic predisposition...
Background Germline mutations affecting the exonuclease domains of POLE and POLD1 predispose to colo...
It is now well established that germline genomic aberrations can underlie high-penetrant familial po...
High-throughput sequencing analysis has accelerated searches for genes associated with risk for colo...
The genetic cause underlying the development of multiple colonic adenomas, the premalignant precurso...
sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype M...
Biallelic germline mutations affecting NTHL1 predispose carriers to adenomatous polyposis and colore...
Biallelic germline mutations affecting NTHL1 predispose carriers to adenomatous polyposis and colore...
SummaryHereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disease caused by ...
Colorectal cancer (CRC) is the third most frequent cancer in the world and has become a major issue ...
Colorectal cancer is one of the most frequent neoplasms and an important cause of mortality in the d...
Colorectal cancer (CRC) is one of the most prevalent malignancies in the Western World and one of th...
Although ~ 25% of colorectal cancer or polyp (CRC/P) cases show familial aggregation, current germli...
BACKGROUND & AIMS: MUTYH-associated polyposis (MAP) is an autosomal recessive disorder caused by mut...
Colorectal cancer is one of the most frequent neoplasms and an important cause of mortality in the d...
The present article summarizes recent developments in the characterization of genetic predisposition...
Background Germline mutations affecting the exonuclease domains of POLE and POLD1 predispose to colo...
It is now well established that germline genomic aberrations can underlie high-penetrant familial po...
High-throughput sequencing analysis has accelerated searches for genes associated with risk for colo...
The genetic cause underlying the development of multiple colonic adenomas, the premalignant precurso...
sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype M...
Biallelic germline mutations affecting NTHL1 predispose carriers to adenomatous polyposis and colore...
Biallelic germline mutations affecting NTHL1 predispose carriers to adenomatous polyposis and colore...
SummaryHereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disease caused by ...
Colorectal cancer (CRC) is the third most frequent cancer in the world and has become a major issue ...
Colorectal cancer is one of the most frequent neoplasms and an important cause of mortality in the d...
Colorectal cancer (CRC) is one of the most prevalent malignancies in the Western World and one of th...
Although ~ 25% of colorectal cancer or polyp (CRC/P) cases show familial aggregation, current germli...
BACKGROUND & AIMS: MUTYH-associated polyposis (MAP) is an autosomal recessive disorder caused by mut...
Colorectal cancer is one of the most frequent neoplasms and an important cause of mortality in the d...
The present article summarizes recent developments in the characterization of genetic predisposition...
Background Germline mutations affecting the exonuclease domains of POLE and POLD1 predispose to colo...
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