Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Nancy Hamel

Showing results (51-60 of 70) with videos related to

Pageof 7
Sort By:
Journal of Medical Genetics|February 19, 2015
A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotypeLili Li, Nancy Hamel, Kristi Baker, et al.
European Journal of Human Genetics : EJHG|December 2, 2010
On the origin and diffusion of BRCA1 c.5266dupC (5382insC) in European populationsNancy Hamel, Bing-Jian Feng, Lenka Foretova, et al.
Cancer Letters|June 24, 2008
Identification and characterization of novel SNPs in CHEK2 in Ashkenazi Jewish men with prostate cancerMarc D Tischkowitz, Ahmet Yilmaz, Long Q Chen, et al.
Nature Genetics|March 30, 2016
Corrigendum: Germline RECQL mutations are associated with breast cancer susceptibilityCezary Cybulski, Jian Carrot-Zhang, Wojciech Kluźniak, et al.
Nature Genetics|April 28, 2015
Germline RECQL mutations are associated with breast cancer susceptibilityCezary Cybulski, Jian Carrot-Zhang, Wojciech Kluźniak, et al.
JAMA|January 6, 2011
DICER1 mutations in familial multinodular goiter with and without ovarian Sertoli-Leydig cell tumorsThomas Rio Frio, Amin Bahubeshi, Chryssa Kanellopoulou, et al.
Acta Neuropathologica|July 16, 2014
Germ-line and somatic DICER1 mutations in pineoblastomaLeanne de Kock, Nelly Sabbaghian, Harriet Druker, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 1, 2005
Macrophage scavenger receptor 1 999C>T (R293X) mutation and risk of prostate cancerQuesta Hope, Sarah Bullock, Christopher Evans, et al.
The Journal of Clinical Investigation|December 6, 2019
DGCR8 microprocessor defect characterizes familial multinodular goiter with schwannomatosisBarbara Rivera, Javad Nadaf, Somayyeh Fahiminiya, et al.
Cancer Research|June 25, 2017
Functionally Null <i>RAD51D</i> Missense Mutation Associates Strongly with Ovarian CarcinomaBarbara Rivera, Massimo Di Iorio, Jessica Frankum, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Journal of Medical Genetics|February 19, 2015
A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotypeLili Li, Nancy Hamel, Kristi Baker, et al.
European Journal of Human Genetics : EJHG|December 2, 2010
On the origin and diffusion of BRCA1 c.5266dupC (5382insC) in European populationsNancy Hamel, Bing-Jian Feng, Lenka Foretova, et al.
Cancer Letters|June 24, 2008
Identification and characterization of novel SNPs in CHEK2 in Ashkenazi Jewish men with prostate cancerMarc D Tischkowitz, Ahmet Yilmaz, Long Q Chen, et al.
Nature Genetics|March 30, 2016
Corrigendum: Germline RECQL mutations are associated with breast cancer susceptibilityCezary Cybulski, Jian Carrot-Zhang, Wojciech Kluźniak, et al.
Nature Genetics|April 28, 2015
Germline RECQL mutations are associated with breast cancer susceptibilityCezary Cybulski, Jian Carrot-Zhang, Wojciech Kluźniak, et al.
JAMA|January 6, 2011
DICER1 mutations in familial multinodular goiter with and without ovarian Sertoli-Leydig cell tumorsThomas Rio Frio, Amin Bahubeshi, Chryssa Kanellopoulou, et al.
Acta Neuropathologica|July 16, 2014
Germ-line and somatic DICER1 mutations in pineoblastomaLeanne de Kock, Nelly Sabbaghian, Harriet Druker, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 1, 2005
Macrophage scavenger receptor 1 999C>T (R293X) mutation and risk of prostate cancerQuesta Hope, Sarah Bullock, Christopher Evans, et al.
The Journal of Clinical Investigation|December 6, 2019
DGCR8 microprocessor defect characterizes familial multinodular goiter with schwannomatosisBarbara Rivera, Javad Nadaf, Somayyeh Fahiminiya, et al.
Cancer Research|June 25, 2017
Functionally Null <i>RAD51D</i> Missense Mutation Associates Strongly with Ovarian CarcinomaBarbara Rivera, Massimo Di Iorio, Jessica Frankum, et al.
Pageof 7