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N Cooper

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Diabetic Medicine : a Journal of the British Diabetic Association|June 14, 2014
Clinical and demographic risk factors associated with mortality during early adulthood in a population-based cohort of childhood-onset type 1 diabetesM N Cooper, N H de Klerk, T W Jones, et al.
Nucleic Acids Research|December 25, 1989
Protein C London 1: recurrent mutation at Arg 169 (CGG----TGG) in the protein C gene causing thrombosisC Grundy, A Chitolie, S Talbot, et al.
Burns : Journal of the International Society for Burn Injuries|April 12, 2022
Quality of life in paediatric burn patients with non-severe burnsAmira Allahham, Matthew N Cooper, Mark W Fear, et al.
The Journal of Pediatrics|October 6, 2022
The December Effect in Pediatric Elective Surgery Utilization: Differences Between Privately and Publicly Insured ChildrenLindsay A Gil, Daryl McLeod, Prasanth Pattisapu, et al.
Human Mutation|January 12, 2005
Meta-analysis of gross insertions causing human genetic disease: novel mutational mechanisms and the role of replication slippageJian-Min Chen, Nadia Chuzhanova, Peter D Stenson, et al.
Journal of Medical Genetics|October 22, 2003
Evaluation of genotype-phenotype correlations in neurofibromatosis type 1B Castle, M E Baser, S M Huson, et al.
Human Genetics|January 1, 1985
An estimate of unique DNA sequence heterozygosity in the human genomeD N Cooper, B A Smith, H J Cooke, et al.
Human Genetics|May 7, 2018
Pronounced maternal parent-of-origin bias for type-1 NF1 microdeletionsLisa Neuhäusler, Anna Summerer, David N Cooper, et al.
Journal of Molecular Evolution|January 1, 1987
The distribution of the dinucleotide CpG and cytosine methylation in the vitellogenin gene familyD N Cooper, S Gerber-Huber, D Nardelli, et al.
Thrombosis Research|September 1, 1990
Molecular genetic analysis of a novel form of haemophilia A characterized by the variable expression of factor VIIIK Wieland, L P Berg, V V Kakkar, et al.
Pageof 144

Showing results (511-520 of 1,439) with videos related to

Sort By:
Pageof 144
Diabetic Medicine : a Journal of the British Diabetic Association|June 14, 2014
Clinical and demographic risk factors associated with mortality during early adulthood in a population-based cohort of childhood-onset type 1 diabetesM N Cooper, N H de Klerk, T W Jones, et al.
Nucleic Acids Research|December 25, 1989
Protein C London 1: recurrent mutation at Arg 169 (CGG----TGG) in the protein C gene causing thrombosisC Grundy, A Chitolie, S Talbot, et al.
Burns : Journal of the International Society for Burn Injuries|April 12, 2022
Quality of life in paediatric burn patients with non-severe burnsAmira Allahham, Matthew N Cooper, Mark W Fear, et al.
The Journal of Pediatrics|October 6, 2022
The December Effect in Pediatric Elective Surgery Utilization: Differences Between Privately and Publicly Insured ChildrenLindsay A Gil, Daryl McLeod, Prasanth Pattisapu, et al.
Human Mutation|January 12, 2005
Meta-analysis of gross insertions causing human genetic disease: novel mutational mechanisms and the role of replication slippageJian-Min Chen, Nadia Chuzhanova, Peter D Stenson, et al.
Journal of Medical Genetics|October 22, 2003
Evaluation of genotype-phenotype correlations in neurofibromatosis type 1B Castle, M E Baser, S M Huson, et al.
Human Genetics|January 1, 1985
An estimate of unique DNA sequence heterozygosity in the human genomeD N Cooper, B A Smith, H J Cooke, et al.
Human Genetics|May 7, 2018
Pronounced maternal parent-of-origin bias for type-1 NF1 microdeletionsLisa Neuhäusler, Anna Summerer, David N Cooper, et al.
Journal of Molecular Evolution|January 1, 1987
The distribution of the dinucleotide CpG and cytosine methylation in the vitellogenin gene familyD N Cooper, S Gerber-Huber, D Nardelli, et al.
Thrombosis Research|September 1, 1990
Molecular genetic analysis of a novel form of haemophilia A characterized by the variable expression of factor VIIIK Wieland, L P Berg, V V Kakkar, et al.
Pageof 144