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Journal of Thrombosis and Haemostasis : JTH|October 5, 2017
Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two casesC Zaninetti, V Santini, M Tiniakou, et al.
Microscopia Electronica Y Biologia Celular : Organo Oficial De Las Sociedades Latinoamericana De Microscopia Electronica E Iberoamericana De Biologia Celular|January 1, 1990
Ultrastructural study of reaggregated culture of brainstem: synaptogenesisE M Lopez, S Peressini, M F Kubke, et al.
Journal of Thrombosis and Haemostasis : JTH|May 5, 2005
Altered cytoskeleton organization in platelets from patients with MYH9-related diseaseI Canobbio, P Noris, A Pecci, et al.
Molecular Endocrinology (Baltimore, Md.)|August 14, 1999
The promoter of the rat 3-hydroxy-3-methylglutaryl coenzyme A reductase gene contains a tissue-specific estrogen-responsive regionL Di Croce, G P Vicent, A Pecci, et al.
Acta Otorhinolaryngologica Italica : Organo Ufficiale Della Societa Italiana Di Otorinolaringologia E Chirurgia Cervico-Facciale|December 14, 2016
Severe to profound deafness may be associated with MYH9-related disease: report of 4 patientsP Canzi, A Pecci, M Manfrin, et al.
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