D N Cooper|S C Lee|S H Barondes - JoVE Visualize

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Journal of Attention Disorders|November 20, 2023

Processing Speed Deficit and Its Relationship with Math Fluency in Children with Attention-Deficit/Hyperactivity DisorderClara S C Lee

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|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.

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.

Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1993

A novel point mutation (Val 297-->Met) in the serine proteinase domain of protein C in a patient with both venous and arterial thromboembolic diseaseD S Millar, A I Wacey, J Voke, et al.

Human Molecular Genetics|December 1, 1994

Disruption of a binding site for hepatocyte nuclear factor 1 in the protein C gene promoter is associated with hereditary thrombophiliaL P Berg, D A Scopes, A Alhaq, et al.

Pageof 146

Showing results (181-190 of 1,454) with videos related to

Sort By:

Pageof 146

Journal of Attention Disorders|November 20, 2023

Processing Speed Deficit and Its Relationship with Math Fluency in Children with Attention-Deficit/Hyperactivity DisorderClara S C Lee

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|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.

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.

Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1993

A novel point mutation (Val 297-->Met) in the serine proteinase domain of protein C in a patient with both venous and arterial thromboembolic diseaseD S Millar, A I Wacey, J Voke, et al.

Human Molecular Genetics|December 1, 1994

Disruption of a binding site for hepatocyte nuclear factor 1 in the protein C gene promoter is associated with hereditary thrombophiliaL P Berg, D A Scopes, A Alhaq, et al.

Pageof 146