Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F GIANNELLI

Showing results (51-60 of 97) with videos related to

Pageof 10
Sort By:
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 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.
Annals of Human Genetics|October 1, 1986
Genetics of Hunter syndrome: carrier detection, new mutations, segregation and linkage analysisD S Chase, A H Morris, A Ballabio, et al.
Human Molecular Genetics|January 1, 1993
Determination of the organisation of coding sequences within the iduronate sulphate sulphatase (IDS) geneR H Flomen, E P Green, P M Green, et al.
Italian Journal of Anatomy and Embryology = Archivio Italiano Di Anatomia Ed Embriologia|January 1, 1996
The blood-flow velocity analysis as a possible method for arterial calibre discovery. A statistical investigation in 108 human subjects by color-Doppler methodC Macchi, C Catini, F Giannelli, et al.
Pageof 10

Showing results (51-60 of 97) with videos related to

Sort By:
Pageof 10
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 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.
Annals of Human Genetics|October 1, 1986
Genetics of Hunter syndrome: carrier detection, new mutations, segregation and linkage analysisD S Chase, A H Morris, A Ballabio, et al.
Human Molecular Genetics|January 1, 1993
Determination of the organisation of coding sequences within the iduronate sulphate sulphatase (IDS) geneR H Flomen, E P Green, P M Green, et al.
Italian Journal of Anatomy and Embryology = Archivio Italiano Di Anatomia Ed Embriologia|January 1, 1996
The blood-flow velocity analysis as a possible method for arterial calibre discovery. A statistical investigation in 108 human subjects by color-Doppler methodC Macchi, C Catini, F Giannelli, et al.
Pageof 10