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F Giannelli

Showing results (61-70 of 140) with videos related to

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Lancet (London, England)|October 31, 1992
Factor VIII gene explains all cases of haemophilia AJ A Naylor, P M Green, C R Rizza, et al.
Genetic Testing|January 1, 1997
Mutation analysis and genetic service: the construction and use of national confidential databases of mutations and pedigreesP M Green, N H Waseem, R D Bagnall, et al.
Human Molecular Genetics|November 1, 1993
Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversionsJ Naylor, A Brinke, S Hassock, et al.
European Journal of Haematology|October 1, 1992
Antenatal diagnosis of haemophilia B by amplification and electrophoresis of an exon fragment with a short deletionR Ljung, P Green, E Sjörin, et al.
Thrombosis and Haemostasis|June 30, 1989
The use of DNA amplification for genetic counselling related diagnosis in haemophilia BT C Tsang, D R Bentley, I M Nilsson, et al.
Journal of Cell Science|February 1, 1978
Changes induced by ultraviolet light in the superhelical DNA of lymphocytes from subjects with xeroderma pigmentosum and normal controlsP R Cook, I A Brazell, S A Pawsey, et al.
Nature: New Biology|September 20, 1972
Induction of galactokinase in fibroblasts from heterozygous and homozygous subjectsF Zacchello, P F Benson, S Brown, et al.
Bollettino Dell'Istituto Sieroterapico Milanese|November 30, 1980
[Epidemiological considerations on 289 cases of tetanus]L Caggese, M R Villa, I Schlacht, et al.
The EMBO Journal|October 1, 1988
A factor IX mutation, verified by direct genomic sequencing, causes haemophilia B by a novel mechanismT C Tsang, D R Bentley, R S Mibashan, et al.
Journal of the American Academy of Dermatology|May 1, 1988
Xeroderma pigmentosum complementation group F in a non-Japanese patientP G Norris, J L Hawk, J A Avery, et al.
Pageof 14

Showing results (61-70 of 140) with videos related to

Sort By:
Pageof 14
Lancet (London, England)|October 31, 1992
Factor VIII gene explains all cases of haemophilia AJ A Naylor, P M Green, C R Rizza, et al.
Genetic Testing|January 1, 1997
Mutation analysis and genetic service: the construction and use of national confidential databases of mutations and pedigreesP M Green, N H Waseem, R D Bagnall, et al.
Human Molecular Genetics|November 1, 1993
Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversionsJ Naylor, A Brinke, S Hassock, et al.
European Journal of Haematology|October 1, 1992
Antenatal diagnosis of haemophilia B by amplification and electrophoresis of an exon fragment with a short deletionR Ljung, P Green, E Sjörin, et al.
Thrombosis and Haemostasis|June 30, 1989
The use of DNA amplification for genetic counselling related diagnosis in haemophilia BT C Tsang, D R Bentley, I M Nilsson, et al.
Journal of Cell Science|February 1, 1978
Changes induced by ultraviolet light in the superhelical DNA of lymphocytes from subjects with xeroderma pigmentosum and normal controlsP R Cook, I A Brazell, S A Pawsey, et al.
Nature: New Biology|September 20, 1972
Induction of galactokinase in fibroblasts from heterozygous and homozygous subjectsF Zacchello, P F Benson, S Brown, et al.
Bollettino Dell'Istituto Sieroterapico Milanese|November 30, 1980
[Epidemiological considerations on 289 cases of tetanus]L Caggese, M R Villa, I Schlacht, et al.
The EMBO Journal|October 1, 1988
A factor IX mutation, verified by direct genomic sequencing, causes haemophilia B by a novel mechanismT C Tsang, D R Bentley, R S Mibashan, et al.
Journal of the American Academy of Dermatology|May 1, 1988
Xeroderma pigmentosum complementation group F in a non-Japanese patientP G Norris, J L Hawk, J A Avery, et al.
Pageof 14