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N M Lindor

Showing results (41-50 of 59) with videos related to

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American Journal of Medical Genetics|August 28, 1995
Uniparental disomy in congenital disorders: a prospective studyN M Lindor, P S Karnes, V V Michels, et al.
Genetic Testing|September 12, 2001
Papillary renal cell carcinoma: analysis of germline mutations in the MET proto-oncogene in a clinic-based populationN M Lindor, C B Dechet, M H Greene, et al.
Genes, Chromosomes & Cancer|January 3, 2001
A search for germline APC mutations in early onset colorectal cancer or familial colorectal cancer with normal DNA mismatch repairL A Boardman, S Schmidt, N M Lindor, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 28, 2003
The APC E1317Q variant in adenomatous polyps and colorectal cancersD Hahnloser, G M Petersen, K Rabe, et al.
Human Molecular Genetics|September 1, 1996
Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancerG Moslein, D J Tester, N M Lindor, et al.
Human Molecular Genetics|July 1, 1993
Autosomal dominant supravalvular aortic stenosis: localization to chromosome 7T M Olson, V V Michels, N M Lindor, et al.
The American Journal of Gastroenterology|August 9, 2003
Desmoid tumors in familial adenomatous polyposis: a pilot project evaluating efficacy of treatment with pirfenidoneN M Lindor, R Dozois, H Nelson, et al.
Molecular Genetics and Metabolism|January 4, 2001
Higher risk of mismatch repair-deficient colorectal cancer in alpha(1)-antitrypsin deficiency carriers and cigarette smokersP Yang, J M Cunningham, K C Halling, et al.
Annals of Internal Medicine|June 20, 1998
Increased risk for cancer in patients with the Peutz-Jeghers syndromeL A Boardman, S N Thibodeau, D J Schaid, et al.
Clinical Genetics|March 1, 1996
Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicismN M Lindor, E M Devries, V V Michels, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|August 28, 1995
Uniparental disomy in congenital disorders: a prospective studyN M Lindor, P S Karnes, V V Michels, et al.
Genetic Testing|September 12, 2001
Papillary renal cell carcinoma: analysis of germline mutations in the MET proto-oncogene in a clinic-based populationN M Lindor, C B Dechet, M H Greene, et al.
Genes, Chromosomes & Cancer|January 3, 2001
A search for germline APC mutations in early onset colorectal cancer or familial colorectal cancer with normal DNA mismatch repairL A Boardman, S Schmidt, N M Lindor, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 28, 2003
The APC E1317Q variant in adenomatous polyps and colorectal cancersD Hahnloser, G M Petersen, K Rabe, et al.
Human Molecular Genetics|September 1, 1996
Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancerG Moslein, D J Tester, N M Lindor, et al.
Human Molecular Genetics|July 1, 1993
Autosomal dominant supravalvular aortic stenosis: localization to chromosome 7T M Olson, V V Michels, N M Lindor, et al.
The American Journal of Gastroenterology|August 9, 2003
Desmoid tumors in familial adenomatous polyposis: a pilot project evaluating efficacy of treatment with pirfenidoneN M Lindor, R Dozois, H Nelson, et al.
Molecular Genetics and Metabolism|January 4, 2001
Higher risk of mismatch repair-deficient colorectal cancer in alpha(1)-antitrypsin deficiency carriers and cigarette smokersP Yang, J M Cunningham, K C Halling, et al.
Annals of Internal Medicine|June 20, 1998
Increased risk for cancer in patients with the Peutz-Jeghers syndromeL A Boardman, S N Thibodeau, D J Schaid, et al.
Clinical Genetics|March 1, 1996
Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicismN M Lindor, E M Devries, V V Michels, et al.
Pageof 6