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F Giannelli

Showing results (81-90 of 140) with videos related to

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Blood|April 15, 1996
A novel DNA inversion causing severe hemophilia AJ A Naylor, P Nicholson, Goodeve Anne, et al.
International Angiology : a Journal of the International Union of Angiology|December 14, 2006
Hemodynamics of the sapheno-femoral complex: an operational diagnosis of proximal femoral valve functionM Cappelli, R Molino Lova, S Ermini, et al.
Human Molecular Genetics|July 1, 1995
Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctionsJ A Naylor, D Buck, P Green, et al.
Journal of Medical Genetics|September 1, 1992
A new strategy for the genetic counselling of diseases of marked mutational heterogeneity: haemophilia B as a modelF Giannelli, S Saad, A J Montandon, et al.
Journal of Thrombosis and Haemostasis : JTH|December 17, 2003
DNA variation in a 13-Mb region including the F9 gene: inferring the genealogical history and causal role of a hemophilia B mutation (IVS 5+13 A-->G)T Anagnostopoulos, A P Morris, K L Ayres, et al.
Thrombosis and Haemostasis|January 23, 1992
Haplotype analysis of identical factor IX mutants using PCRP M Green, A J Montandon, R Ljung, et al.
The Quarterly Journal of Medicine|April 1, 1979
Clinical, genetic and DNA repair studies on a consecutive series of patients with xeroderma pigmentosumS A Pawsey, I A Magnus, C A Ramsay, et al.
Annals of Human Genetics|May 1, 1987
Genetic heterogeneity of X-linked mental retardation with fragile X. Association of tight linkage to factor IX and incomplete penetrance in malesF Giannelli, A H Morris, C Garrett, et al.
Lancet (London, England)|March 16, 1991
Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII geneJ A Naylor, P M Green, A J Montandon, et al.
The EMBO Journal|April 1, 1989
Molecular pathology of haemophilia BP M Green, D R Bentley, R S Mibashan, et al.
Pageof 14

Showing results (81-90 of 140) with videos related to

Sort By:
Pageof 14
Blood|April 15, 1996
A novel DNA inversion causing severe hemophilia AJ A Naylor, P Nicholson, Goodeve Anne, et al.
International Angiology : a Journal of the International Union of Angiology|December 14, 2006
Hemodynamics of the sapheno-femoral complex: an operational diagnosis of proximal femoral valve functionM Cappelli, R Molino Lova, S Ermini, et al.
Human Molecular Genetics|July 1, 1995
Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctionsJ A Naylor, D Buck, P Green, et al.
Journal of Medical Genetics|September 1, 1992
A new strategy for the genetic counselling of diseases of marked mutational heterogeneity: haemophilia B as a modelF Giannelli, S Saad, A J Montandon, et al.
Journal of Thrombosis and Haemostasis : JTH|December 17, 2003
DNA variation in a 13-Mb region including the F9 gene: inferring the genealogical history and causal role of a hemophilia B mutation (IVS 5+13 A-->G)T Anagnostopoulos, A P Morris, K L Ayres, et al.
Thrombosis and Haemostasis|January 23, 1992
Haplotype analysis of identical factor IX mutants using PCRP M Green, A J Montandon, R Ljung, et al.
The Quarterly Journal of Medicine|April 1, 1979
Clinical, genetic and DNA repair studies on a consecutive series of patients with xeroderma pigmentosumS A Pawsey, I A Magnus, C A Ramsay, et al.
Annals of Human Genetics|May 1, 1987
Genetic heterogeneity of X-linked mental retardation with fragile X. Association of tight linkage to factor IX and incomplete penetrance in malesF Giannelli, A H Morris, C Garrett, et al.
Lancet (London, England)|March 16, 1991
Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII geneJ A Naylor, P M Green, A J Montandon, et al.
The EMBO Journal|April 1, 1989
Molecular pathology of haemophilia BP M Green, D R Bentley, R S Mibashan, et al.
Pageof 14