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

Reiner Caspari, S Olschwang, Waltraut Friedl, +8

Human Molecular Genetics

Comparison of Capsule Endoscopy and Magnetic Resonance Imaging for the Detection of Polyps of the Small Intestine in Patients with Familial Adenomatous Polyposis or with Peutz-Jeghers’ Syndrome

Reiner Caspari, M von Falkenhausen, C Krautmacher, +3

Endoscopy

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

Reiner Caspari, Waltraut Friedl, Marion Mandl, +8

The Lancet

Somatic VariantCancer PathologyEarly OnsetFamilial Adenomatous PolyposisGenetics +8

<i>MUTYH</i>‐associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype

Stefan Aretz, Siegfried Uhlhaas, Heike Goergens, +7

International Journal of Cancer

Biallelic MutationsGenetic DisorderMedicineGeneticsPathogenesis +9

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, C. Lamberti, +4

Human Genetics

Genetic DisorderFamilial Adenomatous PolyposisGeneticsApc ProteinPathology +7

Allogeneic Dendritic Cells Fused with Tumor Cells: Preclinical Results and Outcome of a Clinical Phase I/II Trial in Patients with Metastatic Renal Cell Carcinoma

Angela Märten, Sabine Renoth, Thomas Heinicke, +14

Human Gene Therapy

Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis

Stefan Aretz, Siegfried Uhlhaas, Reiner Caspari, +4

European Journal of Human Genetics

Allelic VariantGenetic DisorderApc MutationsGeneticsFamilial Adenomatous Polyposis +6

Familial adenomatous polyposis: Aberrant splicing due to missense or silent mutations in the<i>APC</i>gene

Stefan Aretz, Siegfried Uhlhaas, Yuli Sun, +7

Human Mutation

GeneticsGenetic EpidemiologyPathologyMolecular GeneticsExon 15 +14

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, +8

Gut

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

Marion Mandl, Rainer Paffenholz, Waltraut Friedl, +3

Human Molecular Genetics