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European Journal of Human Genetics : EJHG|August 13, 2002
High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activityFlorent Soubrier, Sabrina Martin, Amalia Alonso, et al.
Annals of Tropical Paediatrics|May 20, 2006
Polymorphisms in genes involved in folate metabolism as risk factors for oedematous severe childhood malnutrition: a hypothesis-generating studyKwesi G Marshall, Sharon Howell, Asha V Badaloo, et al.
Frontiers in Genetics|June 12, 2013
Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthmaLin Li, Michael Kabesch, Emmanuelle Bouzigon, et al.
The Biochemical Journal|February 21, 2002
Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractilityDavid Burton, Hassan Abdulrazzak, Adam Knott, et al.
The International Journal of Cardiovascular Imaging|November 4, 2005
Hypertrophic cardiomyopathy in Noonan Syndrome closely mimics familial hypertrophic cardiomyopathy due to sarcomeric mutationsLucy E Hudsmith, Steffen E Petersen, Jane M Francis, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|February 19, 2013
In vivo mouse cardiac hyperpolarized magnetic resonance spectroscopyMichael S Dodd, Vicky Ball, Rosalind Bray, et al.
European Journal of Human Genetics : EJHG|June 13, 2019
Do health professionals value genomic testing? A discrete choice experiment in inherited cardiovascular diseaseJames Buchanan, Edward Blair, Kate L Thomson, et al.
European Heart Journal|March 20, 2010
DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness modelSarah Wordsworth, José Leal, Edward Blair, et al.
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