Marion Mandl

Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444

Reiner Caspari, S Olschwang, Waltraut Friedl et al. · Human Molecular Genetics · 1995 · 367 citations

Familial adenomatous polyposis: mutation at codon 1309 and early onset of colon cancer

Reiner Caspari, Waltraut Friedl, Marion Mandl et al. · The Lancet · 1994 · 224 citations

Somatic Variant, Cancer Pathology, Early Onset +10

Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposis

Marion Mandl, Rainer Paffenholz, Waltraut Friedl et al. · Human Molecular Genetics · 1994 · 63 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

Predictive diagnosis in familial adenomatous polyposis: evaluation of molecular genetic and ophthalmologic methods.

Reiner Caspari, Waltraut Friedl, T. Böker et al. · PubMed · 1993 · 24 citations

Retinal Pigment Anomalies, Genetic Testing, Ocular Disease +17