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BMJ (Clinical Research Ed.)|September 21, 1996
Familial risks of squamous cell carcinoma of the head and neck: retrospective case-control studyW D Foulkes, J S Brunet, W Sieh, et al.Melanoma Research|December 1, 1996
Cutaneous malignant melanoma in women is uncommonly associated with a family history of melanoma in first-degree relatives: a case-control studyC Cutler, W D Foulkes, J S Brunet, et al.British Journal of Cancer|June 20, 2013
A comparison of the detection of BRCA mutation carriers through the provision of Jewish population-based genetic testing compared with clinic-based genetic testingK A Metcalfe, A Poll, R Royer, et al.Cancer|October 15, 1994
Hereditary and familial ovarian cancer in southern OntarioS A Narod, L Madlensky, L Bradley, et al.Cancer Research|February 10, 2000
Inherited predisposition to pancreatic adenocarcinoma: role of family history and germ-line p16, BRCA1, and BRCA2 mutationsG Lal, G Liu, B Schmocker, et al.Molecular Genetics and Metabolism|February 13, 2001
Genetic factors related to racial variation in plasma levels of insulin-like growth factor-1: implications for premenopausal breast cancer riskH Jernström, W Chu, D Vesprini, et al.Oncogene|June 26, 1997
The familial Wilms' tumour susceptibility gene, FWT1, may not be a tumour suppressor geneN Rahman, L Arbour, P Tonin, et al.Lancet (London, England)|July 13, 1991
Familial breast-ovarian cancer locus on chromosome 17q12-q23S A Narod, J Feunteun, H T Lynch, et al.British Journal of Cancer|July 16, 2014
BRCA1 mRNA levels following a 4-6-week intervention with oral 3,3'-diindolylmethaneJ Kotsopoulos, S Zhang, M Akbari, et al.American Journal of Human Genetics|November 7, 2000
Evaluation of the needs of male carriers of mutations in BRCA1 or BRCA2 who have undergone genetic counselingA Liede, K Metcalfe, D Hanna, et al.Pageof 23