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B Waggoner

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2001
Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of boneV E Kimonis, M J Kovach, B Waggoner, et al.
Nature|September 28, 1995
A second-generation YAC contig map of human chromosome 3R M Gemmill, I Chumakov, P Scott, et al.
Sleep Medicine Reviews|October 21, 2019
Effects of fatigue on teams and their role in 24/7 operationsSiobhan Banks, Lauren Blackwell Landon, Jillian Dorrian, et al.
Genes, Chromosomes & Cancer|December 1, 1994
Integrated YAC contig containing the 3p14.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3BF L Boldog, B Waggoner, T W Glover, et al.
Journal of Sleep Research|October 18, 2019
Exercise before bed does not impact sleep inertia in young healthy malesGrace E Vincent, Charli Sargent, Gregory D Roach, et al.
Prehospital Emergency Care|January 12, 2018
Does Implementation of Biomathematical Models Mitigate Fatigue and Fatigue-related Risks in Emergency Medical Services Operations? A Systematic ReviewFrancine O James, Lauren B Waggoner, Patricia M Weiss, et al.
Oncogene|March 21, 1996
Distinct 3p21.3 deletions in lung cancer and identification of a new human semaphorinJ Roche, F Boldog, M Robinson, et al.
Human Molecular Genetics|February 1, 1997
Chromosome 3p14 homozygous deletions and sequence analysis of FRA3BF Boldog, R M Gemmill, J West, et al.
Molecular Genetics and Metabolism|December 26, 2001
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementiaM J Kovach, B Waggoner, S M Leal, et al.
Physical Review Letters|June 1, 2004
Multistrange baryon production in Au-Au collisions at sqrt[s(NN)]=130 GeVJ Adams, C Adler, M M Aggarwal, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2001
Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of boneV E Kimonis, M J Kovach, B Waggoner, et al.
Nature|September 28, 1995
A second-generation YAC contig map of human chromosome 3R M Gemmill, I Chumakov, P Scott, et al.
Sleep Medicine Reviews|October 21, 2019
Effects of fatigue on teams and their role in 24/7 operationsSiobhan Banks, Lauren Blackwell Landon, Jillian Dorrian, et al.
Genes, Chromosomes & Cancer|December 1, 1994
Integrated YAC contig containing the 3p14.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3BF L Boldog, B Waggoner, T W Glover, et al.
Journal of Sleep Research|October 18, 2019
Exercise before bed does not impact sleep inertia in young healthy malesGrace E Vincent, Charli Sargent, Gregory D Roach, et al.
Prehospital Emergency Care|January 12, 2018
Does Implementation of Biomathematical Models Mitigate Fatigue and Fatigue-related Risks in Emergency Medical Services Operations? A Systematic ReviewFrancine O James, Lauren B Waggoner, Patricia M Weiss, et al.
Oncogene|March 21, 1996
Distinct 3p21.3 deletions in lung cancer and identification of a new human semaphorinJ Roche, F Boldog, M Robinson, et al.
Human Molecular Genetics|February 1, 1997
Chromosome 3p14 homozygous deletions and sequence analysis of FRA3BF Boldog, R M Gemmill, J West, et al.
Molecular Genetics and Metabolism|December 26, 2001
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementiaM J Kovach, B Waggoner, S M Leal, et al.
Physical Review Letters|June 1, 2004
Multistrange baryon production in Au-Au collisions at sqrt[s(NN)]=130 GeVJ Adams, C Adler, M M Aggarwal, et al.
Pageof 2