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R Wilcox

Showing results (441-450 of 791) with videos related to

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American Journal of Medical Genetics. Part A|March 9, 2005
Differentiating campomelic dysplasia from Cumming syndromeValerie Watiker, Ralph S Lachman, William R Wilcox, et al.
Circulation|August 1, 1974
Effect of mitral commissurotomy on right-heart workB R Wilcox, N A Coulter, C L Lucas, et al.
Family Practice|May 16, 2022
Mortality in COVID-19 among women on hormone replacement therapy: a retrospective cohort studyHajira Dambha-Miller, William Hinton, Christopher R Wilcox, et al.
Critical Care (London, England)|May 21, 2026
Costs and complications of extracorporeal membrane oxygenation therapy in Australia and New ZealandKate R Wilcox, Lane Meredith, Aidan Burrell, et al.
The American Journal of Cardiology|April 1, 1986
Maturation of pulmonary input impedance spectrum in infants and children with ventricular septal defectC L Lucas, N F Radke, B R Wilcox, et al.
The American Surgeon|May 1, 1988
A clinical review of patients undergoing resection for pulmonary hamartomaJ D Crouch, B A Keagy, P J Starek, et al.
American Journal of Medical Genetics|May 8, 1999
Lethal osteosclerotic skeletal dysplasia with intracellular inclusion bodiesS G Brodie, R S Lachman, M M McGovern, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4E R Wilcox, L A Everett, X C Li, et al.
Journal of Medical Genetics|February 5, 2002
A single amino acid substitution (D1441Y) in the carboxyl-terminal propeptide of the proalpha1(I) chain of type I collagen results in a lethal variant of osteogenesis imperfecta with features of dense bone diseasesJ M Pace, D Chitayat, M Atkinson, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Marked phenotypic variability in progressive diaphyseal dysplasia (Camurati-Engelmann disease): report of a four-generation pedigree, identification of a mutation in TGFB1, and reviewStephanie E Wallace, Ralph S Lachman, Pertchoui B Mekikian, et al.
Pageof 80

Showing results (441-450 of 791) with videos related to

Sort By:
Pageof 80
American Journal of Medical Genetics. Part A|March 9, 2005
Differentiating campomelic dysplasia from Cumming syndromeValerie Watiker, Ralph S Lachman, William R Wilcox, et al.
Circulation|August 1, 1974
Effect of mitral commissurotomy on right-heart workB R Wilcox, N A Coulter, C L Lucas, et al.
Family Practice|May 16, 2022
Mortality in COVID-19 among women on hormone replacement therapy: a retrospective cohort studyHajira Dambha-Miller, William Hinton, Christopher R Wilcox, et al.
Critical Care (London, England)|May 21, 2026
Costs and complications of extracorporeal membrane oxygenation therapy in Australia and New ZealandKate R Wilcox, Lane Meredith, Aidan Burrell, et al.
The American Journal of Cardiology|April 1, 1986
Maturation of pulmonary input impedance spectrum in infants and children with ventricular septal defectC L Lucas, N F Radke, B R Wilcox, et al.
The American Surgeon|May 1, 1988
A clinical review of patients undergoing resection for pulmonary hamartomaJ D Crouch, B A Keagy, P J Starek, et al.
American Journal of Medical Genetics|May 8, 1999
Lethal osteosclerotic skeletal dysplasia with intracellular inclusion bodiesS G Brodie, R S Lachman, M M McGovern, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4E R Wilcox, L A Everett, X C Li, et al.
Journal of Medical Genetics|February 5, 2002
A single amino acid substitution (D1441Y) in the carboxyl-terminal propeptide of the proalpha1(I) chain of type I collagen results in a lethal variant of osteogenesis imperfecta with features of dense bone diseasesJ M Pace, D Chitayat, M Atkinson, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Marked phenotypic variability in progressive diaphyseal dysplasia (Camurati-Engelmann disease): report of a four-generation pedigree, identification of a mutation in TGFB1, and reviewStephanie E Wallace, Ralph S Lachman, Pertchoui B Mekikian, et al.
Pageof 80