I. van Leeuwen‐Cornelisse

发表

Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis

R. Fodde, R. B. van der Luijt, G. Griffioen, 1997, Human mutation.

Presymptomatic, prenatal, and exclusion testing for Huntington disease using seven closely linked DNA markers.

G. van Ommen, P. Pearson, A. Verwest, 1991, American journal of medical genetics.

Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis.

Inge, J. Kleibeuker, D. Lindhout, 1995, American journal of human genetics.

Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel electrophoresis.

R. Fodde, R. B. van der Luijt, G. Griffioen, 1992, Genomics.

Molecular, cytogenetic, and phenotypic studies of a constitutional reciprocal translocation t(5; I0)(q22; q25) responsible for familial adenomatous polyposis in a Dutch pedigree

R. Fodde, R. B. van der Luijt, H. Vasen, 1995, Genes, chromosomes & cancer.

Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.

P. Møller, R. Fodde, M. Losekoot, 1997, American journal of human genetics.

Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16.

A. Cats, R. Fodde, R. Kolodner, 1996, American journal of human genetics.

Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registry

J. Kleibeuker, M. Breuning, H. Vasen, 2016, Familial Cancer.

Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.

A. Zwinderman, K. Heimdal, P. Møller, 1998, The New England journal of medicine.

The value of screening and central registration of families with familial adenomatous polyposis

G. Griffioen, C. Lamers, H. Vasen, 1990, Diseases of the colon and rectum.

Familial adenomatous polyposis and its clinical surveillance.

F. Nagengast, G. Griffioen, H. Vasen, 1993, Netherlands Journal of Medicine.

Close linkage of a highly polymorphic marker (D5S37) to familial adenomatous polyposis (FAP) and confirmation of FAP localization on chromosome 5q21-q22

G. Griffioen, H. Vasen, C. Tops, 1988, Human Genetics.