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The Journal of Biological Chemistry
|
August 12, 2011
Functional characterization of TNNC1 rare variants identified in dilated cardiomyopathy
Jose Renato Pinto, Jill D Siegfried, Michelle S Parvatiyar, et al.
Clinical and Translational Science
|
October 27, 2010
Late onset sporadic dilated cardiomyopathy caused by a cardiac troponin T mutation
Ana Morales, Jose Renato Pinto, Jill D Siegfried, et al.
Cancer Research
|
August 16, 2008
The relative contribution of point mutations and genomic rearrangements in BRCA1 and BRCA2 in high-risk breast cancer families
Maurizia Dalla Palma, Susan M Domchek, Jill Stopfer, et al.
Journal of Genetic Counseling
|
August 14, 2012
Return of genetic results in the familial dilated cardiomyopathy research project
Jill D Siegfried, Ana Morales, Jessica D Kushner, et al.
American Journal of Human Genetics
|
March 1, 2011
Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy
Nadine Norton, Duanxiang Li, Mark J Rieder, et al.
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of 2
Search research articles
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Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
The Journal of Biological Chemistry
|
August 12, 2011
Functional characterization of TNNC1 rare variants identified in dilated cardiomyopathy
Jose Renato Pinto, Jill D Siegfried, Michelle S Parvatiyar, et al.
Clinical and Translational Science
|
October 27, 2010
Late onset sporadic dilated cardiomyopathy caused by a cardiac troponin T mutation
Ana Morales, Jose Renato Pinto, Jill D Siegfried, et al.
Cancer Research
|
August 16, 2008
The relative contribution of point mutations and genomic rearrangements in BRCA1 and BRCA2 in high-risk breast cancer families
Maurizia Dalla Palma, Susan M Domchek, Jill Stopfer, et al.
Journal of Genetic Counseling
|
August 14, 2012
Return of genetic results in the familial dilated cardiomyopathy research project
Jill D Siegfried, Ana Morales, Jessica D Kushner, et al.
American Journal of Human Genetics
|
March 1, 2011
Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy
Nadine Norton, Duanxiang Li, Mark J Rieder, et al.
Page
of 2