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O El-Maarri

Showing results (1-10 of 21) with videos related to

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Current Topics in Microbiology and Immunology|March 31, 2006
Familial hydatidiform molar pregnancy: the germline imprinting defect hypothesis?O El-Maarri, R Slim
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 23, 2002
Inhibitor development in correlation to factor VIII genotypesJ Oldenburg, O El-Maarri, R Schwaab
British Journal of Haematology|November 11, 1999
Intron 22-specific long PCR for the Xba I polymorphism in the factor VIII geneO El-Maarri, J Oldenburg, S H Cağlayan
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 12, 1999
Intron 22 inversions in the Turkish haemophilia A patients: prevalence and haplotype analysisO El-Maarri, K Kavakli, S H Caglayan
Hamostaseologie|December 4, 2013
F8 genetic analysis strategies when standard approaches failB Pezeshkpoor, A Pavlova, J Oldenburg, et al.
Journal of Thrombosis and Haemostasis : JTH|June 8, 2012
Identification of a third rearrangement at Xq28 that causes severe hemophilia A as a result of homologous recombination between inverted repeatsB Pezeshkpoor, S Rost, J Oldenburg, et al.
British Journal of Haematology|March 21, 1998
Analysis of the two microsatellite repeat polymorphisms of the factor VIII gene in the Turkish populationH Jarjanazi, A A Timur, O El-Maarri, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 5, 2003
Bisulfite-based methylation analysis of imprinted genesS Engemann, O El-Maarri, P Hajkova, et al.
Human Molecular Genetics|January 4, 2001
Methylation profiles of DXPas34 during the onset of X-inactivationM Prissette, O El-Maarri, D Arnaud, et al.
Journal of Thrombosis and Haemostasis : JTH|May 13, 2006
Factor VIII intron-1 inversion: frequency and inhibitor prevalenceJ Schröder, O El-Maarri, R Schwaab, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Current Topics in Microbiology and Immunology|March 31, 2006
Familial hydatidiform molar pregnancy: the germline imprinting defect hypothesis?O El-Maarri, R Slim
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 23, 2002
Inhibitor development in correlation to factor VIII genotypesJ Oldenburg, O El-Maarri, R Schwaab
British Journal of Haematology|November 11, 1999
Intron 22-specific long PCR for the Xba I polymorphism in the factor VIII geneO El-Maarri, J Oldenburg, S H Cağlayan
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 12, 1999
Intron 22 inversions in the Turkish haemophilia A patients: prevalence and haplotype analysisO El-Maarri, K Kavakli, S H Caglayan
Hamostaseologie|December 4, 2013
F8 genetic analysis strategies when standard approaches failB Pezeshkpoor, A Pavlova, J Oldenburg, et al.
Journal of Thrombosis and Haemostasis : JTH|June 8, 2012
Identification of a third rearrangement at Xq28 that causes severe hemophilia A as a result of homologous recombination between inverted repeatsB Pezeshkpoor, S Rost, J Oldenburg, et al.
British Journal of Haematology|March 21, 1998
Analysis of the two microsatellite repeat polymorphisms of the factor VIII gene in the Turkish populationH Jarjanazi, A A Timur, O El-Maarri, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 5, 2003
Bisulfite-based methylation analysis of imprinted genesS Engemann, O El-Maarri, P Hajkova, et al.
Human Molecular Genetics|January 4, 2001
Methylation profiles of DXPas34 during the onset of X-inactivationM Prissette, O El-Maarri, D Arnaud, et al.
Journal of Thrombosis and Haemostasis : JTH|May 13, 2006
Factor VIII intron-1 inversion: frequency and inhibitor prevalenceJ Schröder, O El-Maarri, R Schwaab, et al.
Pageof 3