Marlies Sengteller

Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants

Constanze Pagenstecher, Maria Wehner, Waltraut Friedl et al. · Human Genetics · 2005 · 91 citations

Intronic Variants, Aberrant Splicing, Genetic Disorder +6

Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes

Maria Wehner, Elisabeth Mangold, Marlies Sengteller et al. · European Journal of Human Genetics · 2005 · 37 citations · Full text

Deletion Screening, Medicine, Genetics +8

A modified multiplex PCR assay for detection of large deletions inMSH2 andMLH1

Yaping Wang, Waltraut Friedl, Marlies Sengteller et al. · Human Mutation · 2002 · 37 citations

Familial adenomatous polyposis: A submicroscopic deletion at the APC locus in a family with mentally normal patients

Marion Mandl, Reiner Caspari, Anna Jauch et al. · Human Genetics · 1996 · 35 citations

Family Medicine, Apc Locus, Genetic Disorder +6

Attenuated familial adenomatous polyposis due to a mutation in the 3′ part of the APC gene. A clue for understanding the function of the APC protein

Waltraut Friedl, Stephanie Meuschel, Reiner Caspari et al. · Human Genetics · 1996 · 24 citations

Genetic Disorder, Familial Adenomatous Polyposis, Genetics +9