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L Hopper

Showing results (401-410 of 1,167) with videos related to

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Clinical Genetics|May 15, 2012
Recurrent and founder mutations in the PMS2 geneJ Tomsic, L Senter, S Liyanarachchi, et al.
Gynecologic Oncology|March 18, 2014
Does risk of endometrial cancer for women without a germline mutation in a DNA mismatch repair gene depend on family history of endometrial cancer or colorectal cancer?Rajani Bharati, Mark A Jenkins, Noralane M Lindor, et al.
International Journal of Cancer|June 10, 2010
Risk of endometrial cancer for women diagnosed with HNPCC-related colorectal carcinomaAndreas Obermair, Danny R Youlden, Joanne P Young, et al.
Breast Cancer Research : BCR|April 2, 2022
Population-based estimates of age-specific cumulative risk of breast cancer for pathogenic variants in ATMAnne-Laure Renault, James G Dowty, Jason A Steen, et al.
American Journal of Respiratory and Critical Care Medicine|December 9, 2000
Evidence for genetic associations between asthma, atopy, and bronchial hyperresponsiveness: a study of 8- to 18-yr-old twinsJ R Clarke, M A Jenkins, J L Hopper, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|November 27, 2019
Twins Research Australia: A New Paradigm for Driving Twin ResearchKate Murphy, Janine Lam, Tessa Cutler, et al.
The Journal of Molecular Diagnostics : JMD|July 5, 2011
FMR1 intron 1 methylation predicts FMRP expression in blood of female carriers of expanded FMR1 allelesDavid E Godler, Howard R Slater, Quang M Bui, et al.
Cancer Prevention Research (Philadelphia, Pa.)|October 28, 2010
Constitutional methylation of the BRCA1 promoter is specifically associated with BRCA1 mutation-associated pathology in early-onset breast cancerEe Ming Wong, Melissa C Southey, Stephen B Fox, et al.
Journal of Genetic Counseling|June 11, 2013
Perceived versus predicted risks of colorectal cancer and self-reported colonoscopies by members of mismatch repair gene mutation-carrying families who have declined genetic testingLouisa Flander, Andrew Speirs-Bridge, Alison Rutstein, et al.
Breast Cancer Research and Treatment|August 12, 2009
Contralateral risk-reducing mastectomy in BRCA1 and BRCA2 mutation carriers and other high-risk women in the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (kConFab)Belinda E Kiely, Mark A Jenkins, Joanne M McKinley, et al.
Pageof 117

Showing results (401-410 of 1,167) with videos related to

Sort By:
Pageof 117
Clinical Genetics|May 15, 2012
Recurrent and founder mutations in the PMS2 geneJ Tomsic, L Senter, S Liyanarachchi, et al.
Gynecologic Oncology|March 18, 2014
Does risk of endometrial cancer for women without a germline mutation in a DNA mismatch repair gene depend on family history of endometrial cancer or colorectal cancer?Rajani Bharati, Mark A Jenkins, Noralane M Lindor, et al.
International Journal of Cancer|June 10, 2010
Risk of endometrial cancer for women diagnosed with HNPCC-related colorectal carcinomaAndreas Obermair, Danny R Youlden, Joanne P Young, et al.
Breast Cancer Research : BCR|April 2, 2022
Population-based estimates of age-specific cumulative risk of breast cancer for pathogenic variants in ATMAnne-Laure Renault, James G Dowty, Jason A Steen, et al.
American Journal of Respiratory and Critical Care Medicine|December 9, 2000
Evidence for genetic associations between asthma, atopy, and bronchial hyperresponsiveness: a study of 8- to 18-yr-old twinsJ R Clarke, M A Jenkins, J L Hopper, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|November 27, 2019
Twins Research Australia: A New Paradigm for Driving Twin ResearchKate Murphy, Janine Lam, Tessa Cutler, et al.
The Journal of Molecular Diagnostics : JMD|July 5, 2011
FMR1 intron 1 methylation predicts FMRP expression in blood of female carriers of expanded FMR1 allelesDavid E Godler, Howard R Slater, Quang M Bui, et al.
Cancer Prevention Research (Philadelphia, Pa.)|October 28, 2010
Constitutional methylation of the BRCA1 promoter is specifically associated with BRCA1 mutation-associated pathology in early-onset breast cancerEe Ming Wong, Melissa C Southey, Stephen B Fox, et al.
Journal of Genetic Counseling|June 11, 2013
Perceived versus predicted risks of colorectal cancer and self-reported colonoscopies by members of mismatch repair gene mutation-carrying families who have declined genetic testingLouisa Flander, Andrew Speirs-Bridge, Alison Rutstein, et al.
Breast Cancer Research and Treatment|August 12, 2009
Contralateral risk-reducing mastectomy in BRCA1 and BRCA2 mutation carriers and other high-risk women in the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (kConFab)Belinda E Kiely, Mark A Jenkins, Joanne M McKinley, et al.
Pageof 117