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D N Cooper

Showing results (121-130 of 205) with videos related to

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Prenatal Diagnosis|November 1, 1992
Prenatal exclusion of haemophilia A and carrier testing by direct detection of a disease lesionM Schwartz, D N Cooper, D S Millar, et al.
Journal of Medical Genetics|July 1, 1995
Population differences in the frequency of the factor V Leiden variant among people with clinically symptomatic protein C deficiencyP J Hallam, D S Millar, M Krawczak, et al.
Human Genetics|March 1, 1992
A novel missense mutation in the antithrombin III gene (Ser349----Pro) causing recurrent venous thrombosisC B Grundy, S Holding, D S Millar, et al.
Human Genetics|August 1, 1991
Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) geneJ Reiss, D N Cooper, J Bal, et al.
Human Genetics|May 1, 1991
Carrier detection in haemophilia A by direct analysis of factor VIII gene lesionsD S Millar, P J Green, B Zoll, et al.
Thorax|February 1, 1981
Relationship between asthma and gastro-oesophageal refluxR J Goodall, J E Earis, D N Cooper, et al.
Thrombosis and Haemostasis|July 1, 1997
Inherited factor VII deficiency: molecular genetics and pathophysiologyD N Cooper, D S Millar, A Wacey, et al.
British Journal of Haematology|June 1, 1993
A molecular model of the serine protease domain of activated protein C: application to the study of missense mutations causing protein C deficiencyA I Wacey, S Pemberton, D N Cooper, et al.
Nucleic Acids Research|May 11, 1983
Chicken lens delta-crystallin gene expression and methylation in several non-lens tissuesD J Bower, L H Errington, D N Cooper, et al.
Gene|September 7, 2000
Promoter shuffling has occurred during the evolution of the vertebrate growth hormone geneN A Chuzhanova, M Krawczak, L A Nemytikova, et al.
Pageof 21

Showing results (121-130 of 205) with videos related to

Sort By:
Pageof 21
Prenatal Diagnosis|November 1, 1992
Prenatal exclusion of haemophilia A and carrier testing by direct detection of a disease lesionM Schwartz, D N Cooper, D S Millar, et al.
Journal of Medical Genetics|July 1, 1995
Population differences in the frequency of the factor V Leiden variant among people with clinically symptomatic protein C deficiencyP J Hallam, D S Millar, M Krawczak, et al.
Human Genetics|March 1, 1992
A novel missense mutation in the antithrombin III gene (Ser349----Pro) causing recurrent venous thrombosisC B Grundy, S Holding, D S Millar, et al.
Human Genetics|August 1, 1991
Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) geneJ Reiss, D N Cooper, J Bal, et al.
Human Genetics|May 1, 1991
Carrier detection in haemophilia A by direct analysis of factor VIII gene lesionsD S Millar, P J Green, B Zoll, et al.
Thorax|February 1, 1981
Relationship between asthma and gastro-oesophageal refluxR J Goodall, J E Earis, D N Cooper, et al.
Thrombosis and Haemostasis|July 1, 1997
Inherited factor VII deficiency: molecular genetics and pathophysiologyD N Cooper, D S Millar, A Wacey, et al.
British Journal of Haematology|June 1, 1993
A molecular model of the serine protease domain of activated protein C: application to the study of missense mutations causing protein C deficiencyA I Wacey, S Pemberton, D N Cooper, et al.
Nucleic Acids Research|May 11, 1983
Chicken lens delta-crystallin gene expression and methylation in several non-lens tissuesD J Bower, L H Errington, D N Cooper, et al.
Gene|September 7, 2000
Promoter shuffling has occurred during the evolution of the vertebrate growth hormone geneN A Chuzhanova, M Krawczak, L A Nemytikova, et al.
Pageof 21