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Journal of Medical Genetics|August 1, 1985
Gene deletion in an Italian haemophilia B subjectF Bernardi, L del Senno, R Barbieri, et al.
Blood|May 1, 1987
Factor XII gene alteration in Hageman trait detected by TaqI restriction enzymeF Bernardi, G Marchetti, P Patracchini, et al.
Biochemical and Biophysical Research Communications|November 30, 1984
Human leukemia K562 cells: relationship between hemin-mediated erythroid induction, cell proliferation and expression of c-abl and c-myc oncogenesR Gambari, L del Senno, R Piva, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 14, 2004
How to evaluate phenotype-genotype relationship in rare coagulation haemorrhagic disorders: examples from FVII deficiencyF Bernardi, G Marchetti, A Dolce, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 14, 2004
Clinical picture and management of congenital factor VII deficiencyG Mariani, A Dolce, G Marchetti, et al.
Human Genetics|January 1, 1993
A polymorphism in the 5' region of coagulation factor VII gene (F7) caused by an inserted decanucleotideG Marchetti, P Patracchini, M Papacchini, et al.
Human Genetics|December 1, 1988
Assignment of human coagulation factor XII (fXII) to chromosome 5 by cDNA hybridization to DNA from somatic cell hybridsF Citarella, M Tripodi, A Fantoni, et al.
Human Genetics|November 1, 1992
Characterization and mapping of the 5' portion of von Willebrand factor pseudogeneP Patracchini, G Marchetti, V Aiello, et al.
Blood|August 26, 1998
Molecular mechanisms of FVII deficiency: expression of mutations clustered in the IVS7 donor splice site of factor VII geneM Pinotti, R Toso, R Redaelli, et al.
Thrombosis and Haemostasis|August 28, 2002
Reduced activation of the Gla19Ala FX variant via the extrinsic coagulation pathway results in symptomatic CRMred FX deficiencyM Pinotti, G Marchetti, M Baroni, et al.
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