J-P Mecklin - JoVE Visualize

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Anticancer Research|July 1, 1994

The epidemiology of endometrial cancer in hereditary nonpolyposis colorectal cancerH F Vasen, P Watson, J P Mecklin, et al.

Human Mutation|April 13, 1999

Mutation sharing, predominant involvement of the MLH1 gene and description of four novel mutations in hereditary nonpolyposis colorectal cancer. Mutations in brief no. 144. OnlineM Holmberg, P Kristo, R B Chadwicks, et al.

Journal of Medical Genetics|July 17, 2007

Direct contact in inviting high-risk members of hereditary colon cancer families to genetic counselling and DNA testingK Aktan-Collan, A Haukkala, K Pylvänäinen, et al.

Gynecologic Oncology|September 5, 2001

The clinical features of ovarian cancer in hereditary nonpolyposis colorectal cancerP Watson, R Bützow, H T Lynch, et al.

Gastroenterology|April 28, 2000

Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancerH J Järvinen, M Aarnio, H Mustonen, et al.

Cancer Research|August 15, 1992

Evidence that the MCC-APC gene region in 5q21 is not the site for susceptibility to hereditary nonpolyposis colorectal carcinomaP Peltomäki, P Sistonen, J P Mecklin, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 21, 1994

Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer familiesM Nyström-Lahti, P Sistonen, J P Mecklin, et al.

Gut|February 3, 2007

Is gastric cancer part of the tumour spectrum of hereditary non-polyposis colorectal cancer? A molecular genetic studyA Gylling, W M Abdel-Rahman, M Juhola, et al.

Diseases of the Colon and Rectum|June 1, 1995

Frequency of hereditary nonpolyposis colorectal cancer. A prospective multicenter study in FinlandJ P Mecklin, H J Järvinen, A Hakkiluoto, et al.

International Journal of Cancer|April 3, 1999

Cancer risk in mutation carriers of DNA-mismatch-repair genesM Aarnio, R Sankila, E Pukkala, et al.

Pageof 10

Showing results (61-70 of 100) with videos related to

Sort By:

Pageof 10

Anticancer Research|July 1, 1994

The epidemiology of endometrial cancer in hereditary nonpolyposis colorectal cancerH F Vasen, P Watson, J P Mecklin, et al.

Human Mutation|April 13, 1999

Mutation sharing, predominant involvement of the MLH1 gene and description of four novel mutations in hereditary nonpolyposis colorectal cancer. Mutations in brief no. 144. OnlineM Holmberg, P Kristo, R B Chadwicks, et al.

Journal of Medical Genetics|July 17, 2007

Direct contact in inviting high-risk members of hereditary colon cancer families to genetic counselling and DNA testingK Aktan-Collan, A Haukkala, K Pylvänäinen, et al.

Gynecologic Oncology|September 5, 2001

The clinical features of ovarian cancer in hereditary nonpolyposis colorectal cancerP Watson, R Bützow, H T Lynch, et al.

Gastroenterology|April 28, 2000

Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancerH J Järvinen, M Aarnio, H Mustonen, et al.

Cancer Research|August 15, 1992

Evidence that the MCC-APC gene region in 5q21 is not the site for susceptibility to hereditary nonpolyposis colorectal carcinomaP Peltomäki, P Sistonen, J P Mecklin, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 21, 1994

Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer familiesM Nyström-Lahti, P Sistonen, J P Mecklin, et al.

Gut|February 3, 2007

Is gastric cancer part of the tumour spectrum of hereditary non-polyposis colorectal cancer? A molecular genetic studyA Gylling, W M Abdel-Rahman, M Juhola, et al.

Diseases of the Colon and Rectum|June 1, 1995

Frequency of hereditary nonpolyposis colorectal cancer. A prospective multicenter study in FinlandJ P Mecklin, H J Järvinen, A Hakkiluoto, et al.

International Journal of Cancer|April 3, 1999

Cancer risk in mutation carriers of DNA-mismatch-repair genesM Aarnio, R Sankila, E Pukkala, et al.

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