Matthias Jungck

Muir-Torre Phenotype Has a Frequency of DNA Mismatch-Repair-Gene Mutations Similar to That in Hereditary Nonpolyposis Colorectal Cancer Families Defined by the Amsterdam Criteria

Roland Kruse, Arno Rütten, Christof Lamberti et al. · The American Journal of Human Genetics · 1998 · 234 citations · Full text

Genome Instability, Somatic Variant, Genetic Disorder +10

Hereditary nonpolyposis colorectal cancer: Frequent occurrence of large genomic deletions in <i>MSH2</i> and <i>MLH1</i> genes

Yaping Wang, Waltraut Friedl, Christof Lamberti et al. · International Journal of Cancer · 2002 · 105 citations

DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2

Elke Holinski‐Feder, Y Müller-Koch, Waltraut Friedl et al. · Journal of Biochemical and Biophysical Methods · 2001 · 94 citations

Dhplc Mutation Analysis, Somatic Variant, Medicine +9

Frequent 4-bp deletion in exon 9 of theSMAD4/MADH4 gene in familial juvenile polyposis patients

Waltraut Friedl, Roland Kruse, Siegfried Uhlhaas et al. · Genes Chromosomes and Cancer · 1999 · 94 citations

Mendelian Disorder, Familial Juvenile Polyposis, Exon 9 +13

Microsatellite instability—a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer

C. Lamberti, Roland Kruse, Corina Ruelfs et al. · Gut · 1999 · 91 citations · Full text