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D R Bentley

Showing results (31-40 of 88) with videos related to

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Genomics|May 1, 1993
Exon structure of the human dystrophin geneR G Roberts, A J Coffey, M Bobrow, et al.
Genomics|December 1, 1992
A panel of human chromosome 22-specific sequence tagged sitesJ E Collins, L A Everett, D R Bentley, 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.
Genomics|August 1, 1992
Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCRR G Roberts, A J Coffey, M Bobrow, 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.
Immunogenetics|January 1, 1985
DNA polymorphism of the C2 and factor B genes. Detection of a restriction fragment length polymorphism which subdivides haplotypes carrying the C2C and factor B F allelesS J Cross, J H Edwards, D R Bentley, et al.
Nature|January 19, 1984
A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor BM C Carroll, R D Campbell, D R Bentley, et al.
Genomics|August 1, 1990
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy geneS Abbs, R G Roberts, C G Mathew, et al.
Lancet (London, England)|December 22, 1990
Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNAR G Roberts, D R Bentley, T F Barby, et al.
Pageof 9

Showing results (31-40 of 88) with videos related to

Sort By:
Pageof 9
Genomics|May 1, 1993
Exon structure of the human dystrophin geneR G Roberts, A J Coffey, M Bobrow, et al.
Genomics|December 1, 1992
A panel of human chromosome 22-specific sequence tagged sitesJ E Collins, L A Everett, D R Bentley, 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.
Genomics|August 1, 1992
Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCRR G Roberts, A J Coffey, M Bobrow, 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.
Immunogenetics|January 1, 1985
DNA polymorphism of the C2 and factor B genes. Detection of a restriction fragment length polymorphism which subdivides haplotypes carrying the C2C and factor B F allelesS J Cross, J H Edwards, D R Bentley, et al.
Nature|January 19, 1984
A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor BM C Carroll, R D Campbell, D R Bentley, et al.
Genomics|August 1, 1990
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy geneS Abbs, R G Roberts, C G Mathew, et al.
Lancet (London, England)|December 22, 1990
Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNAR G Roberts, D R Bentley, T F Barby, et al.
Pageof 9