Sfoglia per Autore
Mostrati risultati da 1 a 7 di 7
The DNA pooling technique applied to the mutational screening of human congenital afibrinogenemia : identification of 3 novel mutations
2003 L. Monaldini, R. Asselta, M. Malcovati, M.L. Tenchini, S. Duga
Uniparental disomy of chromosome 4 including a novel deletion in the FGA gene that causes congenital afibrinogenemia
2004 S. Spena, R. Asselta, S. Duga, L. Monaldini, M. Malcovati, M.L. Tenchini
Fibrinogen Mumbai: impaired secretion due to a novel missense mutation in the Bbeta-chain gene
2005 L. Monaldini, S. Duga, R. Asselta, M. Malcovati, M.L. Tenchini
Congenital afibrinogenemia : two novel fibrinogen gene mutations identified in two patients from Iran
2006 L. Monaldini, R. Asselta, S. Duga, F. Peyvandi, M. Malcovati, M.L. Tenchini
Two novel homozygous mutations in the fibrinogen genes identified in two Iranian afibrinogenemic patients
2006 L. Monaldini, S. Duga, R. Asselta, F. Peyvandi, M. Karimi, M. Malcovati, M.L. Tenchini
Fibrinogen Mumbai : intracellular retention due to a novel G434D mutation in the Bbeta-chain gene
2006 L. Monaldini, R. Asselta, S. Duga, F. Peyvandi, K. Ghosh, M. Malcovati, M.L. Tenchini
Mutational screening of six afibrinogenemic patients : identification and characterization of four novel molecular defects
2007 L. Monaldini, R. Asselta, S. Duga, F. Peyvandi, M. Karimi, M. Malcovati, M.L. Tenchini
Mostrati risultati da 1 a 7 di 7
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