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F Giannelli

Showing results (51-60 of 140) with videos related to

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Thrombosis and Haemostasis|May 1, 1994
First report on UK database of haemophilia B mutations and pedigrees. UK Haemophilia CentresS Saad, G Rowley, L Tagliavacca, et al.
Molecular Biology & Medicine|April 1, 1988
Partial deletion by illegitimate recombination of the factor IX gene in a haemophilia B family with two inhibitor patientsP M Green, D R Bentley, R S Mibashan, et al.
Human Molecular Genetics|January 1, 1993
Analysis of factor VIII mRNA reveals defects in everyone of 28 haemophilia A patientsJ A Naylor, P M Green, C R Rizza, et al.
Prenatal Diagnosis|May 1, 1984
Mitomycin C induced chromosome damage in fetal blood cultures and prenatal diagnosis of Fanconi's anaemiaJ Shipley, C H Rodeck, C Garrett, et al.
Nucleic Acids Research|May 11, 1989
Direct detection of point mutations by mismatch analysis: application to haemophilia BA J Montandon, P M Green, F Giannelli, et al.
British Journal of Haematology|August 12, 2008
Haemophilia A mutations in the UK: results of screening one-third of the populationP M Green, R D Bagnall, N H Waseem, et al.
Radiation Research|October 1, 1981
Xeroderma Pigmentosum and medulloblastoma: chromosomal damage to lymphocytes during radiotherapyF Giannelli, J Avery, P E Polani, et al.
The Journal of Investigative Dermatology|April 1, 1978
A human subject with a new defect in repair of ultraviolet damageC F Arlett, A R Lehmann, F Giannelli, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1991
Genetics and molecular biology of haemophilias A and BP M Green, A J Montandon, D R Bentley, et al.
PCR Methods and Applications|April 1, 1994
Mutation detection by fluorescent chemical cleavage: application to hemophilia BI I Haris, P M Green, D R Bentley, et al.
Pageof 14

Showing results (51-60 of 140) with videos related to

Sort By:
Pageof 14
Thrombosis and Haemostasis|May 1, 1994
First report on UK database of haemophilia B mutations and pedigrees. UK Haemophilia CentresS Saad, G Rowley, L Tagliavacca, et al.
Molecular Biology & Medicine|April 1, 1988
Partial deletion by illegitimate recombination of the factor IX gene in a haemophilia B family with two inhibitor patientsP M Green, D R Bentley, R S Mibashan, et al.
Human Molecular Genetics|January 1, 1993
Analysis of factor VIII mRNA reveals defects in everyone of 28 haemophilia A patientsJ A Naylor, P M Green, C R Rizza, et al.
Prenatal Diagnosis|May 1, 1984
Mitomycin C induced chromosome damage in fetal blood cultures and prenatal diagnosis of Fanconi's anaemiaJ Shipley, C H Rodeck, C Garrett, et al.
Nucleic Acids Research|May 11, 1989
Direct detection of point mutations by mismatch analysis: application to haemophilia BA J Montandon, P M Green, F Giannelli, et al.
British Journal of Haematology|August 12, 2008
Haemophilia A mutations in the UK: results of screening one-third of the populationP M Green, R D Bagnall, N H Waseem, et al.
Radiation Research|October 1, 1981
Xeroderma Pigmentosum and medulloblastoma: chromosomal damage to lymphocytes during radiotherapyF Giannelli, J Avery, P E Polani, et al.
The Journal of Investigative Dermatology|April 1, 1978
A human subject with a new defect in repair of ultraviolet damageC F Arlett, A R Lehmann, F Giannelli, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1991
Genetics and molecular biology of haemophilias A and BP M Green, A J Montandon, D R Bentley, et al.
PCR Methods and Applications|April 1, 1994
Mutation detection by fluorescent chemical cleavage: application to hemophilia BI I Haris, P M Green, D R Bentley, et al.
Pageof 14