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F Giannelli

Showing results (101-110 of 140) with videos related to

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Journal of Medical Genetics|March 1, 1989
Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studiesM A Patton, F Giannelli, A J Francis, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Analysis of the haemophilia A mutation in sporadic patients registered at the Royal London Hospital and their familiesL Tagliavacca, G Rowley, P M Green, et al.
Current Studies in Hematology and Blood Transfusion|January 1, 1991
A new strategy for carrier and prenatal diagnosis and molecular studies in haemophilia BA J Montandon, P M Green, D R Bentley, et al.
Nucleic Acids Research|June 11, 1990
The incidence and distribution of CpG----TpG transitions in the coagulation factor IX gene. A fresh look at CpG mutational hotspotsP M Green, A J Montandon, D R Bentley, et al.
Clinical and Experimental Rheumatology|January 28, 1998
Frequency of bcl-2 rearrangement in patients with mixed cryoglobulinemia and HCV-positive liver diseasesA L Zignego, F Giannelli, M E Marrocchi, et al.
Nature|May 12, 1983
Gene deletions in patients with haemophilia B and anti-factor IX antibodiesF Giannelli, K H Choo, D J Rees, et al.
Italian Journal of Anatomy and Embryology = Archivio Italiano Di Anatomia Ed Embriologia|April 1, 1996
The inner diameter of human intracranial vertebral artery by color Doppler methodC Macchi, F Giannelli, F Cecchi, et al.
Human Genetics|July 1, 1990
Two factor IX mutations in the family of an isolated haemophilia B patient: direct carrier diagnosis by amplification mismatch detection (AMD)A J Montandon, P M Green, D R Bentley, et al.
Nature|August 8, 1970
Evidence that the Xg locus is inactivated in structurally abnormal X chromosomesP E Polani, R Angell, F Giannelli, et al.
European Journal of Haematology|October 1, 1991
Moderate haemophilia B in a female carrier caused by preferential inactivation of the paternal X chromosomeS Kling, A J Coffey, R Ljung, et al.
Pageof 14

Showing results (101-110 of 140) with videos related to

Sort By:
Pageof 14
Journal of Medical Genetics|March 1, 1989
Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studiesM A Patton, F Giannelli, A J Francis, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Analysis of the haemophilia A mutation in sporadic patients registered at the Royal London Hospital and their familiesL Tagliavacca, G Rowley, P M Green, et al.
Current Studies in Hematology and Blood Transfusion|January 1, 1991
A new strategy for carrier and prenatal diagnosis and molecular studies in haemophilia BA J Montandon, P M Green, D R Bentley, et al.
Nucleic Acids Research|June 11, 1990
The incidence and distribution of CpG----TpG transitions in the coagulation factor IX gene. A fresh look at CpG mutational hotspotsP M Green, A J Montandon, D R Bentley, et al.
Clinical and Experimental Rheumatology|January 28, 1998
Frequency of bcl-2 rearrangement in patients with mixed cryoglobulinemia and HCV-positive liver diseasesA L Zignego, F Giannelli, M E Marrocchi, et al.
Nature|May 12, 1983
Gene deletions in patients with haemophilia B and anti-factor IX antibodiesF Giannelli, K H Choo, D J Rees, et al.
Italian Journal of Anatomy and Embryology = Archivio Italiano Di Anatomia Ed Embriologia|April 1, 1996
The inner diameter of human intracranial vertebral artery by color Doppler methodC Macchi, F Giannelli, F Cecchi, et al.
Human Genetics|July 1, 1990
Two factor IX mutations in the family of an isolated haemophilia B patient: direct carrier diagnosis by amplification mismatch detection (AMD)A J Montandon, P M Green, D R Bentley, et al.
Nature|August 8, 1970
Evidence that the Xg locus is inactivated in structurally abnormal X chromosomesP E Polani, R Angell, F Giannelli, et al.
European Journal of Haematology|October 1, 1991
Moderate haemophilia B in a female carrier caused by preferential inactivation of the paternal X chromosomeS Kling, A J Coffey, R Ljung, et al.
Pageof 14