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Blood Cells, Molecules & Diseases|April 3, 2007
Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCRAlexis Proust, Benoît Guillet, Capucine Picard, et al.
Haematologica|February 25, 2010
Investigating the key membrane protein changes during in vitro erythropoiesis of protein 4.2 (-) cells (mutations Chartres 1 and 2)Emile van den Akker, Timothy J Satchwell, Stephanie Pellegrin, et al.
Blood|January 5, 2008
Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin AAshley M Toye, Rosalind C Williamson, Moudji Khanfar, et al.
American Journal of Hematology|August 19, 2011
Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian populationRoberta Russo, Antonella Gambale, Maria Rosaria Esposito, et al.
Blood|January 18, 2003
A band 3-based macrocomplex of integral and peripheral proteins in the RBC membraneLesley J Bruce, Roland Beckmann, M Leticia Ribeiro, et al.
Journal of Pediatric Hematology/Oncology|August 13, 2005
Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in a cohort of French childrenBrigitte Bader-Meunier, Guy Leverger, Gil Tchernia, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
A second locus mapping to 2q35-36 for familial pseudohyperkalaemiaMassimo Carella, Adamo Pio d'Adamo, Sabine Grootenboer-Mignot, et al.
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