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7. The use of fluorescence flow cytometry in the characterization of Bernard-Soulier syndrome and Glanzmann's thrombasthenia. Fabris F; Casonato A; Randi ML; Luzzatto G; De Silvestro G; Ongaro G; Girolami A Haematologica; 1989; 74(1):39-44. PubMed ID: 2498181 [TBL] [Abstract][Full Text] [Related]
8. Inherited disorders of platelets and megakaryocytes. Nurden AT; Pico M; Heilmann E; Jallu V; Hourdillé P Prog Clin Biol Res; 1990; 356():333-46. PubMed ID: 2217448 [No Abstract] [Full Text] [Related]
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17. Molecular abnormalities in Glanzmann's thrombasthenia, Bernard-Soulier syndrome, and platelet-type von Willebrand's disease. Clemetson KJ; Clemetson JM Curr Opin Hematol; 1994 Sep; 1(5):388-93. PubMed ID: 9371310 [TBL] [Abstract][Full Text] [Related]
18. Genetic testing in the diagnostic evaluation of inherited platelet disorders. Nurden AT; Fiore M; Pillois X; Nurden P Semin Thromb Hemost; 2009 Mar; 35(2):204-12. PubMed ID: 19408193 [TBL] [Abstract][Full Text] [Related]
19. Talin does not associate exclusively with alpha 2b beta 3 integrin in activated human platelets. Escolar G; Diaz-Ricart M; White JG J Lab Clin Med; 1995 May; 125(5):597-607. PubMed ID: 7537787 [TBL] [Abstract][Full Text] [Related]