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M C King

Showing results (161-170 of 186) with videos related to

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American Journal of Human Genetics|April 1, 1993
THRA1 and D17S183 flank an interval of < 4 cM for the breast-ovarian cancer gene (BRCA1) on chromosome 17q21A M Bowcock, L A Anderson, L S Friedman, et al.
Cancer Research|July 15, 1995
Mutation analysis of the BRCA1 gene in ovarian cancersH Takahashi, K Behbakht, P E McGovern, et al.
American Journal of Human Genetics|December 1, 1995
Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish familiesL S Friedman, C I Szabo, E A Ostermeyer, et al.
Human Molecular Genetics|November 16, 2001
Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1T L Young, E Ives, E Lynch, et al.
Science (New York, N.Y.)|March 21, 1997
Genetic information and the workplace: legislative approaches and policy changesK Rothenberg, B Fuller, M Rothstein, et al.
JAMA|November 17, 2001
Tamoxifen and breast cancer incidence among women with inherited mutations in BRCA1 and BRCA2: National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) Breast Cancer Prevention TrialM C King, S Wieand, K Hale, et al.
Cancer Research|December 15, 1994
The search for BRCA1L S Friedman, E A Ostermeyer, E D Lynch, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 3, 2001
Identification of Id4 as a regulator of BRCA1 expression by using a ribozyme-library-based inverse genomics approachC Beger, L N Pierce, M Kruger, et al.
Human Genetics|November 1, 1991
Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene regionR V Lebo, P F Chance, P J Dyck, et al.
Nature Genetics|March 1, 1996
BRCA1 is secreted and exhibits properties of a graninR A Jensen, M E Thompson, T L Jetton, et al.
Pageof 19

Showing results (161-170 of 186) with videos related to

Sort By:
Pageof 19
American Journal of Human Genetics|April 1, 1993
THRA1 and D17S183 flank an interval of < 4 cM for the breast-ovarian cancer gene (BRCA1) on chromosome 17q21A M Bowcock, L A Anderson, L S Friedman, et al.
Cancer Research|July 15, 1995
Mutation analysis of the BRCA1 gene in ovarian cancersH Takahashi, K Behbakht, P E McGovern, et al.
American Journal of Human Genetics|December 1, 1995
Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish familiesL S Friedman, C I Szabo, E A Ostermeyer, et al.
Human Molecular Genetics|November 16, 2001
Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1T L Young, E Ives, E Lynch, et al.
Science (New York, N.Y.)|March 21, 1997
Genetic information and the workplace: legislative approaches and policy changesK Rothenberg, B Fuller, M Rothstein, et al.
JAMA|November 17, 2001
Tamoxifen and breast cancer incidence among women with inherited mutations in BRCA1 and BRCA2: National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) Breast Cancer Prevention TrialM C King, S Wieand, K Hale, et al.
Cancer Research|December 15, 1994
The search for BRCA1L S Friedman, E A Ostermeyer, E D Lynch, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 3, 2001
Identification of Id4 as a regulator of BRCA1 expression by using a ribozyme-library-based inverse genomics approachC Beger, L N Pierce, M Kruger, et al.
Human Genetics|November 1, 1991
Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene regionR V Lebo, P F Chance, P J Dyck, et al.
Nature Genetics|March 1, 1996
BRCA1 is secreted and exhibits properties of a graninR A Jensen, M E Thompson, T L Jetton, et al.
Pageof 19