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Results: 1-3 |
Results: 3
A boy with venous thrombosis, homozygous for factor V Leiden, prothrombin G20210A and MTHFR C667T mutations, but belonging to an asymptomatic family
Authors: Soria, JM Quintana, R Vallve, C Iruin, G Cortes, C Fontcuberta, J
Citation: Jm. Soria et al., A boy with venous thrombosis, homozygous for factor V Leiden, prothrombin G20210A and MTHFR C667T mutations, but belonging to an asymptomatic family, HAEMATOLOG, 85(11), 2000, pp. 1230-1232
A 1063G -> A mutation in exon 12 of glycoprotein (GP)IIb associated with athrombasthenic phenotype: mutation analysis of [324E]GPIIb
Authors: Tao, JM Arias-Salgado, EG Gonzalez-Manchon, C Iruin, G Butta, N Ayuso, MS Parrilla, R
Citation: Jm. Tao et al., A 1063G -> A mutation in exon 12 of glycoprotein (GP)IIb associated with athrombasthenic phenotype: mutation analysis of [324E]GPIIb, BR J HAEM, 111(3), 2000, pp. 965-973
Truncation of glycoprotein (GP) IIIa (Delta 616-762) prevents complex formation with GPIIb: Novel mutation in exon 11 of GPIIIa associated with thrombasthenia
Authors: Ferrer, M Tao, JM Iruin, G Sanchez-Ayuso, M Gonzalez-Rodriguez, J Parrilla, R Gonzalez-Manchon, C
Citation: M. Ferrer et al., Truncation of glycoprotein (GP) IIIa (Delta 616-762) prevents complex formation with GPIIb: Novel mutation in exon 11 of GPIIIa associated with thrombasthenia, BLOOD, 92(12), 1998, pp. 4712-4720
Risultati: 1-3 |