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D R Bentley

Showing results (41-50 of 88) with videos related to

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Trends in Genetics : TIG|November 20, 1998
Coordination of human genome sequencing via a consensus framework mapD R Bentley, K D Pruitt, P Deloukas, et al.
Journal of Medical Genetics|September 1, 1992
A new strategy for the genetic counselling of diseases of marked mutational heterogeneity: haemophilia B as a modelF Giannelli, S Saad, A J Montandon, et al.
American Journal of Human Genetics|August 1, 1991
Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytesR G Roberts, T F Barby, E Manners, et al.
The EMBO Journal|April 1, 1989
Molecular pathology of haemophilia BP M Green, D R Bentley, R S Mibashan, et al.
Nucleic Acids Research|October 25, 1991
A MseI polymorphism in exon 48 of the dystrophin geneS C Yau, R G Roberts, D R Bentley, 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.
Nucleic Acids Research|January 25, 1989
Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophyR G Roberts, C G Cole, K A Hart, et al.
Genomics|July 1, 1992
Detection of point mutations and a gross deletion in six Hunter syndrome patientsR H Flomen, P M Green, D R Bentley, et al.
The Journal of Experimental Medicine|June 1, 1992
A variable number of tandem repeats locus within the human complement C2 gene is associated with a retroposon derived from a human endogenous retrovirusZ B Zhu, S L Hsieh, D R Bentley, et al.
Genomics|December 1, 1992
Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplificationC G Cole, K Patel, J Shipley, et al.
Pageof 9

Showing results (41-50 of 88) with videos related to

Sort By:
Pageof 9
Trends in Genetics : TIG|November 20, 1998
Coordination of human genome sequencing via a consensus framework mapD R Bentley, K D Pruitt, P Deloukas, et al.
Journal of Medical Genetics|September 1, 1992
A new strategy for the genetic counselling of diseases of marked mutational heterogeneity: haemophilia B as a modelF Giannelli, S Saad, A J Montandon, et al.
American Journal of Human Genetics|August 1, 1991
Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytesR G Roberts, T F Barby, E Manners, et al.
The EMBO Journal|April 1, 1989
Molecular pathology of haemophilia BP M Green, D R Bentley, R S Mibashan, et al.
Nucleic Acids Research|October 25, 1991
A MseI polymorphism in exon 48 of the dystrophin geneS C Yau, R G Roberts, D R Bentley, 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.
Nucleic Acids Research|January 25, 1989
Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophyR G Roberts, C G Cole, K A Hart, et al.
Genomics|July 1, 1992
Detection of point mutations and a gross deletion in six Hunter syndrome patientsR H Flomen, P M Green, D R Bentley, et al.
The Journal of Experimental Medicine|June 1, 1992
A variable number of tandem repeats locus within the human complement C2 gene is associated with a retroposon derived from a human endogenous retrovirusZ B Zhu, S L Hsieh, D R Bentley, et al.
Genomics|December 1, 1992
Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplificationC G Cole, K Patel, J Shipley, et al.
Pageof 9