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Genome Research
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May 26, 2007
Systematic analysis of genetic alterations in tumors using Cancer Genome WorkBench (CGWB)
Jinghui Zhang, Richard P Finney, William Rowe, et al.
International Journal of Cancer
|
September 24, 2004
CHEK2:1100delC and female breast cancer in the United States
Lutécia H Mateus Pereira, Alice J Sigurdson, Michele M Doody, et al.
BMC Genetics
|
October 6, 2007
The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-control association studies
Lutécia H Mateus Pereira, Marbin A Pineda, William H Rowe, et al.
Genetic Epidemiology
|
October 6, 2005
Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping
Nathan A Ellis, Tomas Kirchhoff, Nandita Mitra, et al.
Cancer
|
July 13, 2002
A natural history of melanomas and dysplastic nevi: an atlas of lesions in melanoma-prone families
Margaret A Tucker, Mary C Fraser, Alisa M Goldstein, et al.
Biopreservation and Biobanking
|
May 22, 2014
Meeting research needs with postmortem biospecimen donation: summary of recommendations for postmortem recovery of normal human biospecimens for research
Neil R Mucci, Helen M Moore, Lori E Brigham, et al.
Cancer
|
November 6, 2004
Heterogeneity of risk for melanoma and pancreatic and digestive malignancies: a melanoma case-control study
Joni L Rutter, Christina M Bromley, Alisa M Goldstein, et al.
Human Mutation
|
July 23, 2003
Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals
Joni L Rutter, Amelia M Smith, Michael R Dávila, et al.
Radiation Research
|
January 14, 2009
Thyroid nodules, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in Kazakhstan
Alice J Sigurdson, Charles E Land, Parveen Bhatti, et al.
Human Mutation
|
May 3, 2006
The ATM missense mutation p.Ser49Cys (c.146C>G) and the risk of breast cancer
Denise L Stredrick, Montserrat Garcia-Closas, Marbin A Pineda, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 46) with videos related to
Sort By:
Page
of 5
Genome Research
|
May 26, 2007
Systematic analysis of genetic alterations in tumors using Cancer Genome WorkBench (CGWB)
Jinghui Zhang, Richard P Finney, William Rowe, et al.
International Journal of Cancer
|
September 24, 2004
CHEK2:1100delC and female breast cancer in the United States
Lutécia H Mateus Pereira, Alice J Sigurdson, Michele M Doody, et al.
BMC Genetics
|
October 6, 2007
The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-control association studies
Lutécia H Mateus Pereira, Marbin A Pineda, William H Rowe, et al.
Genetic Epidemiology
|
October 6, 2005
Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping
Nathan A Ellis, Tomas Kirchhoff, Nandita Mitra, et al.
Cancer
|
July 13, 2002
A natural history of melanomas and dysplastic nevi: an atlas of lesions in melanoma-prone families
Margaret A Tucker, Mary C Fraser, Alisa M Goldstein, et al.
Biopreservation and Biobanking
|
May 22, 2014
Meeting research needs with postmortem biospecimen donation: summary of recommendations for postmortem recovery of normal human biospecimens for research
Neil R Mucci, Helen M Moore, Lori E Brigham, et al.
Cancer
|
November 6, 2004
Heterogeneity of risk for melanoma and pancreatic and digestive malignancies: a melanoma case-control study
Joni L Rutter, Christina M Bromley, Alisa M Goldstein, et al.
Human Mutation
|
July 23, 2003
Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals
Joni L Rutter, Amelia M Smith, Michael R Dávila, et al.
Radiation Research
|
January 14, 2009
Thyroid nodules, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in Kazakhstan
Alice J Sigurdson, Charles E Land, Parveen Bhatti, et al.
Human Mutation
|
May 3, 2006
The ATM missense mutation p.Ser49Cys (c.146C>G) and the risk of breast cancer
Denise L Stredrick, Montserrat Garcia-Closas, Marbin A Pineda, et al.
Page
of 5