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MYH9 related disease: a novel missense Ala95Asp mutation of the MYH9 gene.
de Rocco D, Heller PG, Girotto G, Pastore A, Glembotsky AC, Marta RF, Bozzi V, Pecci A, Molinas FC, Savoia A. de Rocco D, et al. Among authors: molinas fc. Platelets. 2009 Dec;20(8):598-602. doi: 10.3109/09537100903349620. Platelets. 2009. PMID: 19860543 Free article.
International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country.
Glembotsky AC, Marta RF, Pecci A, De Rocco D, Gnan C, Espasandin YR, Goette NP, Negro F, Noris P, Savoia A, Balduini CL, Molinas FC, Heller PG. Glembotsky AC, et al. Among authors: molinas fc. J Thromb Haemost. 2012 Aug;10(8):1653-61. doi: 10.1111/j.1538-7836.2012.04805.x. J Thromb Haemost. 2012. PMID: 22672365 Free article.
76 results