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Human Mutation|May 28, 2010
HGV2009 meeting: bigger and better studies provide more answers and more questionsKatherine Reekie, Andres Metspalu, Stephen J Chanock, et al.
European Journal of Human Genetics : EJHG|November 24, 2020
Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participantsLiis Leitsalu, Marili Palover, Timo Tõnis Sikka, et al.
European Journal of Oral Sciences|June 25, 2010
Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patientsTiit Nikopensius, Stefanie Birnbaum, Kerstin U Ludwig, et al.
Personalized Medicine|May 12, 2018
Reporting incidental findings of genomic disorder-associated copy number variants to unselected biobank participantsLiis Leitsalu, Helene Alavere, Sébastien Jacquemont, et al.
European Journal of Human Genetics : EJHG|November 14, 2018
Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health recordsTõnis Tasa, Kristi Krebs, Mart Kals, et al.
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