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British Journal of Haematology|August 16, 2005
Clinical and molecular variability in congenital dyserythropoietic anaemia type IHannah Tamary, Orly Dgany, Alexis Proust, et al.European Journal of Human Genetics : EJHG|June 26, 2003
CATSPER2, a human autosomal nonsyndromic male infertility geneNili Avidan, Hannah Tamary, Orly Dgany, et al.Nature Communications|May 23, 2013
Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channelsJuliette Albuisson, Swetha E Murthy, Michael Bandell, et al.European Journal of Haematology|July 29, 2010
Frequency of congenital dyserythropoietic anemias in EuropeHermann Heimpel, Andreas Matuschek, Momin Ahmed, et al.American Journal of Human Genetics|November 9, 2010
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemiaLionel Arnaud, Carole Saison, Virginie Helias, et al.Nature Genetics|June 30, 2009
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type IIKlaus Schwarz, Achille Iolascon, Fatima Verissimo, et al.Blood|March 13, 2013
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1Immacolata Andolfo, Seth L Alper, Lucia De Franceschi, et al.American Journal of Human Genetics|November 16, 2002
Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1Orly Dgany, Nili Avidan, Jean Delaunay, et al.Pageof 6