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Genomics|August 10, 1995
Generation of a transcription map at the HSD17B locus centromeric to BRCA1 at 17q21J M Rommens, F Durocher, J McArthur, et al.Breast Cancer Research and Treatment|June 9, 2000
RT-PCR amplification of CK19 mRNA in the blood of breast cancer patients: correlation with established prognostic parametersH J Kahn, L Y Yang, J Blondal, et al.Nature Genetics|January 1, 1994
Epidermolytic palmoplantar keratoderma cosegregates with a keratin 9 mutation in a pedigree with breast and ovarian cancerD Torchard, C Blanchet-Bardon, O Serova, et al.Human Molecular Genetics|April 10, 1999
Mismatch repair gene defects contribute to the genetic basis of double primary cancers of the colorectum and endometriumA L Millar, T Pal, L Madlensky, et al.Current Oncology (Toronto, Ont.)|November 11, 2020
A pan-Canadian prospective study of young women with breast cancer: the rationale and protocol design for the RUBY studyM L Quan, I A Olivotto, N N Baxter, et al.The American Journal of Surgical Pathology|October 19, 1999
Immunohistochemistry for hMLH1 and hMSH2: a practical test for DNA mismatch repair-deficient tumorsV A Marcus, L Madlensky, R Gryfe, et al.Hereditary Cancer in Clinical Practice|February 5, 2016
Recurrent mutations of BRCA1, BRCA2 and PALB2 in the population of breast and ovarian cancer patients in Southern PolandP Wojcik, M Jasiowka, E Strycharz, et al.Cancer|June 1, 1997
A descriptive study of BRCA1 testing and reactions to disclosure of test resultsH T Lynch, S J Lemon, C Durham, et al.JAMA|June 26, 1996
BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomesC Lerman, S Narod, K Schulman, et al.British Journal of Cancer|January 22, 2004
Germline truncating mutations in both MSH2 and BRCA2 in a single kindredI Thiffault, N Hamel, T Pal, et al.Pageof 5