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Plos One|November 13, 2012
Increased serum hepcidin levels in subjects with the metabolic syndrome: a population studyNicola Martinelli, Michela Traglia, Natascia Campostrini, et al.
Blood|September 22, 2010
Inherited genetic susceptibility to monoclonal B-cell lymphocytosisDalemari Crowther-Swanepoel, Tanguy Corre, Amy Lloyd, et al.
European Journal of Human Genetics : EJHG|December 1, 2019
A bird's-eye view of Italian genomic variation through whole-genome sequencingMassimiliano Cocca, Caterina Barbieri, Maria Pina Concas, et al.
Human Molecular Genetics|October 2, 2002
Deletion of the mental retardation gene Gdi1 impairs associative memory and alters social behavior in micePatrizia D'Adamo, Hans Welzl, Stavros Papadimitriou, et al.
Blood|July 13, 2021
Relationship between clone metrics and clinical outcome in clonal cytopeniaAnna Gallì, Gabriele Todisco, Eulalia Catamo, et al.
Blood|April 21, 2017
Clinical significance of somatic mutation in unexplained blood cytopeniaLuca Malcovati, Anna Gallì, Erica Travaglino, et al.
Pflugers Archiv : European Journal of Physiology|December 5, 2016
Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urineTanguy Corre, Eric Olinger, Sarah E Harris, et al.
Plos One|August 13, 2013
Genome wide association analysis of a founder population identified TAF3 as a gene for MCHC in humansGiorgio Pistis, Shawntel U Okonkwo, Michela Traglia, et al.
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