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H Cohn

Showing results (751-760 of 962) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|January 1, 1983
Cloning of the Vibrio harveyi luciferase genes: use of a synthetic oligonucleotide probeD H Cohn, R C Ogden, J N Abelson, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Dominant TRPV4 mutations in nonlethal and lethal metatropic dysplasiaNatalia Camacho, Deborah Krakow, Sharlin Johnykutty, et al.
The Annals of Thoracic Surgery|May 30, 2006
Replacement of the quadricuspid aortic valve: strategy to avoid complete heart blockPaul A Pirundini, Jorge M Balaguer, Kevin J Lilly, et al.
Metabolism: Clinical and Experimental|March 1, 1981
Compartmental body composition of cancer patients by measurement of total body nitrogen, potassium, and waterS H Cohn, W Gartenhaus, A Sawitsky, et al.
Health Promotion Practice|April 26, 2006
Childhood asthma surveillance by community coalitionsJohn R Meurer, Livia Navon, Stephen C Redd, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|July 1, 1991
Ischemic injury before heart transplantation does not cause coronary arteriopathy in experimental isograftsP Masetti, V J DiSesa, F J Schoen, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|March 5, 2003
Biological vs. mechanical aortic root replacementJohn G Byrne, Tomas Gudbjartsson, Alexandros N Karavas, et al.
Human Mutation|February 6, 1998
Identification of five novel mutations in cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasiaJ Loughlin, C Irven, Z Mustafa, et al.
Genomics|December 1, 1993
Genetic linkage of mild pseudoachondroplasia (PSACH) to markers in the pericentromeric region of chromosome 19M D Briggs, I M Rasmussen, J L Weber, et al.
American Journal of Human Genetics|June 23, 1998
Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22D Krakow, K Reinker, B Powell, et al.
Pageof 97

Showing results (751-760 of 962) with videos related to

Sort By:
Pageof 97
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1983
Cloning of the Vibrio harveyi luciferase genes: use of a synthetic oligonucleotide probeD H Cohn, R C Ogden, J N Abelson, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Dominant TRPV4 mutations in nonlethal and lethal metatropic dysplasiaNatalia Camacho, Deborah Krakow, Sharlin Johnykutty, et al.
The Annals of Thoracic Surgery|May 30, 2006
Replacement of the quadricuspid aortic valve: strategy to avoid complete heart blockPaul A Pirundini, Jorge M Balaguer, Kevin J Lilly, et al.
Metabolism: Clinical and Experimental|March 1, 1981
Compartmental body composition of cancer patients by measurement of total body nitrogen, potassium, and waterS H Cohn, W Gartenhaus, A Sawitsky, et al.
Health Promotion Practice|April 26, 2006
Childhood asthma surveillance by community coalitionsJohn R Meurer, Livia Navon, Stephen C Redd, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|July 1, 1991
Ischemic injury before heart transplantation does not cause coronary arteriopathy in experimental isograftsP Masetti, V J DiSesa, F J Schoen, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|March 5, 2003
Biological vs. mechanical aortic root replacementJohn G Byrne, Tomas Gudbjartsson, Alexandros N Karavas, et al.
Human Mutation|February 6, 1998
Identification of five novel mutations in cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasiaJ Loughlin, C Irven, Z Mustafa, et al.
Genomics|December 1, 1993
Genetic linkage of mild pseudoachondroplasia (PSACH) to markers in the pericentromeric region of chromosome 19M D Briggs, I M Rasmussen, J L Weber, et al.
American Journal of Human Genetics|June 23, 1998
Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22D Krakow, K Reinker, B Powell, et al.
Pageof 97