M. Cayouette

发表

Distribution of 13 truncating mutations in the neurofibromatosis 1 gene.

R. Heim, L. Kam-Morgan, C. Binnie, 1995, Human molecular genetics.

Hepatoblastoma and APC gene mutation in familial adenomatous polyposis.

G. Petersen, S. Hamilton, M. Cayouette, 1996, Gut.

Attenuated familial adenomatous polyposis (AFAP) a phenotypically and genotypically distinctive variant of FAP

T. Smyrk, M. Cayouette, M. Luce, 1995, Cancer.

Phenotypic Expression of Disease in Families That Have Mutations in the 5 Region of the Adenomatous Polyposis Coli Gene

G. Petersen, S. Hamilton, M. Cayouette, 1997, Annals of Internal Medicine.

Rapid identification of RT-PCR clones containing translation-terminating mutations.

C. Boland, L. Kam-Morgan, C. Binnie, 1997, Mutation research.

In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer.

Sajeev P. Cherian, M. Hawn, L. Kam-Morgan, 1995, Gastroenterology.

Homozygous inactivation of the NF1 gene in bone marrow cells from children with neurofibromatosis type 1 and malignant myeloid disorders.

M. Cayouette, M. Luce, K. Shannon, 1997, The New England journal of medicine.

Genetic alterations and epithelial dysplasia in juvenile polyposis syndrome and sporadic juvenile polyps.

C. Moskaluk, A. Rashid, B. Rezai, 1997, The American journal of pathology.

Mutational analysis of patients with neurofibromatosis, type 1 (NF1) and malignant myeloid disorders using a protein truncation assay.

M. Cayouette, M. Luce, K. Shannon, 1995 .

Identification of DNA mismatch repair gene mutations in hereditary nonpolyposis colon cancer patients

L. Kam-Morgan, C. Binnie, M. Cayouette, 1996, International journal of cancer.

Hepatoblastoma andAPCgenemutation in familial adenomatous polyposis

G. Petersen, M. Cayouette, F. Giardiello, 1996 .