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M Acquila

Showing results (11-20 of 27) with videos related to

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Thrombosis and Haemostasis|April 1, 1993
Two novel mutations at 373 codon of FVIII gene detected by DGGEM Acquila, D Caprino, M Pecorara, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 4, 2008
MLPA assay in F8 gene mutation screeningM Acquila, M Pasino, M Di Duca, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 30, 2002
Mutation analysis is an essential strategy in the genetic counselling of sporadic haemophilia B familiesM P Bicocchi, M Pasino, F Bottini, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 10, 2001
A new strategy for prenatal diagnosis in a sporadic haemophilia B familyM Acquila, F Bottini, A Valetto, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 19, 2009
Multiplex ligation-dependent probe amplification to detect a large deletion within the von Willebrand geneM Acquila, F Bottini, M DI Duca, et al.
European Journal of Haematology|July 29, 2000
A homozygosity state for 20210A prothrombin variant in a young woman as cause of a deep venous thrombosis during pregnancyM Acquila, M P Bicocchi, P G Mori, et al.
Haematologica|April 6, 1999
A rapid prenatal diagnosis of hemophilia A by DNA analysis on crude chorionic villus biopsyM Acquila, M P Bicocchi, F Bottini, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 31, 2004
Germ-line origin of intron 1 inversion in two haemophilia A familiesM Acquila, M Pasino, C Santoro, et al.
Thrombosis and Haemostasis|April 1, 1994
Factor VIII S373L: mutation at P1' site confers thrombin cleavage resistance, causing mild haemophilia AD J Johnson, S Pemberton, M Acquila, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 1, 2004
Identification of mutations in exon 14 including five novelties in 13 Italian patients with haemophilia AM Acquila, M Pasino, T Lanza, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Thrombosis and Haemostasis|April 1, 1993
Two novel mutations at 373 codon of FVIII gene detected by DGGEM Acquila, D Caprino, M Pecorara, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 4, 2008
MLPA assay in F8 gene mutation screeningM Acquila, M Pasino, M Di Duca, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 30, 2002
Mutation analysis is an essential strategy in the genetic counselling of sporadic haemophilia B familiesM P Bicocchi, M Pasino, F Bottini, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 10, 2001
A new strategy for prenatal diagnosis in a sporadic haemophilia B familyM Acquila, F Bottini, A Valetto, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 19, 2009
Multiplex ligation-dependent probe amplification to detect a large deletion within the von Willebrand geneM Acquila, F Bottini, M DI Duca, et al.
European Journal of Haematology|July 29, 2000
A homozygosity state for 20210A prothrombin variant in a young woman as cause of a deep venous thrombosis during pregnancyM Acquila, M P Bicocchi, P G Mori, et al.
Haematologica|April 6, 1999
A rapid prenatal diagnosis of hemophilia A by DNA analysis on crude chorionic villus biopsyM Acquila, M P Bicocchi, F Bottini, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 31, 2004
Germ-line origin of intron 1 inversion in two haemophilia A familiesM Acquila, M Pasino, C Santoro, et al.
Thrombosis and Haemostasis|April 1, 1994
Factor VIII S373L: mutation at P1' site confers thrombin cleavage resistance, causing mild haemophilia AD J Johnson, S Pemberton, M Acquila, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 1, 2004
Identification of mutations in exon 14 including five novelties in 13 Italian patients with haemophilia AM Acquila, M Pasino, T Lanza, et al.
Pageof 3