H. Mueller

Report of an International Survey of Molecular Genetic Testing Laboratories

M. Somerville, D. Barton, D. Taruscio, 2007, Public Health Genomics.

A de novo MLH1 germ line mutation in a 31‐year‐old colorectal cancer patient

G. Marra, K. Heinimann, M. Plášilová, 2006, Genes, chromosomes & cancer.

Familial colorectal cancer: eleven years of data from a registry program in Switzerland

J. Jiricny, E. Laczko, G. Marra, 2011, Familial Cancer.

Evidence for genetic anticipation in hereditary non-polyposis colorectal cancer

P. Hutter, K. Heinimann, Claudine Rey Berthod, 2005, Human Genetics.

Whole-gene APC deletions cause classical familial adenomatous polyposis, but not attenuated polyposis or “multiple” colorectal adenomas

L. Lipton, O. Sieber, W. Bodmer, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Prevalence of MYH germline mutations in Swiss APC mutation‐negative polyposis patients

P. Chappuis, P. Hutter, J. Luz, 2006, International journal of cancer.

Evidence for breast cancer as an integral part of lynch syndrome

G. Marra, K. Heinimann, M. Buser, 2012, Genes, chromosomes & cancer.

Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers.

S. Ollila, G. Marra, K. Heinimann, 2006, Cancer research.

Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers.

G. Marra, K. Heinimann, P. Peltomaki, 2006, Cancer research.

Evidence for breast cancer as an integral part of lynch syndrome

G. Marra, K. Heinimann, M. Buser, 2012, Genes, chromosomes & cancer.