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V Reid Sutton

Showing results (121-130 of 184) with videos related to

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Genome Research|July 15, 2016
The ethics of conducting molecular autopsies in cases of sudden death in the youngAmy L McGuire, Quianta Moore, Mary Majumder, et al.
Molecular Genetics and Metabolism|September 20, 2015
Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United StatesMarcus J Miller, Lindsay C Burrage, James B Gibson, et al.
Journal of Clinical Psychology in Medical Settings|January 28, 2024
Psychosocial Outcomes of Pain and Pain Management in Adults with Osteogenesis Imperfecta: A Qualitative StudyWhitney S Shepherd, Andrew D Wiese, Hannah E Cho, et al.
Disability and Health Journal|June 23, 2026
Sociodemographic and clinical predictors of resilience in individuals with osteogenesis imperfectaMadeline Hawkins, Emily Strouphauer, Ryan McCarty, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 9, 2018
A metabolomic map of Zellweger spectrum disorders reveals novel disease biomarkersMichael F Wangler, Leroy Hubert, Taraka R Donti, et al.
Advances in Therapy|February 28, 2026
Pathways to Facilitate Early Recognition and Diagnosis of HypochondroplasiaMelita Irving, Elena Greco, Alessandra Cocca, et al.
Molecular Genetics and Metabolism|August 24, 2020
Untargeted metabolomics as an unbiased approach to the diagnosis of inborn errors of metabolism of the non-oxidative branch of the pentose phosphate pathwayBrian J Shayota, Taraka R Donti, Jing Xiao, et al.
Disability and Rehabilitation|June 6, 2024
Resilience and coping: a qualitative analysis of cognitive and behavioral factors in adults with osteogenesis ImperfectaHannah E Cho, Whitney S Shepherd, Gianna M Colombo, et al.
American Journal of Medical Genetics. Part A|November 30, 2019
Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome)Nurit Assia Batzir, Jennifer E Posey, Xiaofei Song, et al.
American Journal of Human Genetics|March 1, 2016
DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow SyndromeJanson J White, Juliana F Mazzeu, Alexander Hoischen, et al.
Pageof 19

Showing results (121-130 of 184) with videos related to

Sort By:
Pageof 19
Genome Research|July 15, 2016
The ethics of conducting molecular autopsies in cases of sudden death in the youngAmy L McGuire, Quianta Moore, Mary Majumder, et al.
Molecular Genetics and Metabolism|September 20, 2015
Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United StatesMarcus J Miller, Lindsay C Burrage, James B Gibson, et al.
Journal of Clinical Psychology in Medical Settings|January 28, 2024
Psychosocial Outcomes of Pain and Pain Management in Adults with Osteogenesis Imperfecta: A Qualitative StudyWhitney S Shepherd, Andrew D Wiese, Hannah E Cho, et al.
Disability and Health Journal|June 23, 2026
Sociodemographic and clinical predictors of resilience in individuals with osteogenesis imperfectaMadeline Hawkins, Emily Strouphauer, Ryan McCarty, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 9, 2018
A metabolomic map of Zellweger spectrum disorders reveals novel disease biomarkersMichael F Wangler, Leroy Hubert, Taraka R Donti, et al.
Advances in Therapy|February 28, 2026
Pathways to Facilitate Early Recognition and Diagnosis of HypochondroplasiaMelita Irving, Elena Greco, Alessandra Cocca, et al.
Molecular Genetics and Metabolism|August 24, 2020
Untargeted metabolomics as an unbiased approach to the diagnosis of inborn errors of metabolism of the non-oxidative branch of the pentose phosphate pathwayBrian J Shayota, Taraka R Donti, Jing Xiao, et al.
Disability and Rehabilitation|June 6, 2024
Resilience and coping: a qualitative analysis of cognitive and behavioral factors in adults with osteogenesis ImperfectaHannah E Cho, Whitney S Shepherd, Gianna M Colombo, et al.
American Journal of Medical Genetics. Part A|November 30, 2019
Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome)Nurit Assia Batzir, Jennifer E Posey, Xiaofei Song, et al.
American Journal of Human Genetics|March 1, 2016
DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow SyndromeJanson J White, Juliana F Mazzeu, Alexander Hoischen, et al.
Pageof 19