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Nature Biotechnology|May 10, 2000
Universal DNA array detection of small insertions and deletions in BRCA1 and BRCA2R Favis, J P Day, N P Gerry, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|October 7, 2010
Double heterozygosity in the BRCA1 and BRCA2 genes in the Jewish populationO Lavie, S Narod, F Lejbkowicz, et al.Human Pathology|April 1, 1995
Clinicopathological relevance of the association between gastrointestinal and sebaceous neoplasms: the Muir-Torre syndromeF Paraf, D Sasseville, A K Watters, et al.Journal of Consulting and Clinical Psychology|June 1, 1997
The influence of psychological distress on use of genetic testing for cancer riskC Lerman, M D Schwartz, T H Lin, et al.Human Molecular Genetics|September 1, 1994
The gene for hereditary breast-ovarian cancer, BRCA1, maps distal to EDH17B2 in chromosome region 17q12-q21P Tonin, O Serova, J Simard, et al.Cancer Research|October 18, 2000
BRCA1 promoter region hypermethylation in ovarian carcinoma: a population-based studyR L Baldwin, E Nemeth, H Tran, et al.Surgical Oncology|July 27, 1999
Breast cancer and organochlorines: a marker for susceptibility?M A Musgrave, K J Aronson, S Narod, et al.World Journal of Surgery|January 1, 1994
Hereditary breast cancer and family cancer syndromesH T Lynch, J Lynch, T Conway, et al.Revue Neurologique|January 1, 1991
[Genetics of neurofibromatosis: recent progress and prospects]M Maillet-Vioud, S Narod, D Assouline, et al.Pageof 5