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Charles A Williams

Showing results (31-40 of 37) with videos related to

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Advanced Healthcare Materials|June 13, 2025
Bioengineered Human Cardiac Ventricular Model with Transmural Helical RemodelingNisa P Williams, Kevin M Beussman, John R Foster, et al.
Skeletal Muscle|June 2, 2018
TRAPPC11 and GOSR2 mutations associate with hypoglycosylation of α-dystroglycan and muscular dystrophyAustin A Larson, Peter R Baker, Miroslav P Milev, et al.
The British Journal of Ophthalmology|November 25, 2010
The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats diseaseJohane M Robitaille, Binyou Zheng, Karin Wallace, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2019
Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locusFederica Maria Valente, Angela Sparago, Andrea Freschi, et al.
American Journal of Human Genetics|November 27, 2010
Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problemsMelissa B Ramocki, Magdalena Bartnik, Przemyslaw Szafranski, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Overlapping spectra of SMAD4 mutations in juvenile polyposis (JP) and JP-HHT syndromeCarol Gallione, Arthur S Aylsworth, Jill Beis, et al.
American Journal of Human Genetics|October 11, 2011
Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorderMichael E Talkowski, Sureni V Mullegama, Jill A Rosenfeld, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Advanced Healthcare Materials|June 13, 2025
Bioengineered Human Cardiac Ventricular Model with Transmural Helical RemodelingNisa P Williams, Kevin M Beussman, John R Foster, et al.
Skeletal Muscle|June 2, 2018
TRAPPC11 and GOSR2 mutations associate with hypoglycosylation of α-dystroglycan and muscular dystrophyAustin A Larson, Peter R Baker, Miroslav P Milev, et al.
The British Journal of Ophthalmology|November 25, 2010
The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats diseaseJohane M Robitaille, Binyou Zheng, Karin Wallace, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2019
Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locusFederica Maria Valente, Angela Sparago, Andrea Freschi, et al.
American Journal of Human Genetics|November 27, 2010
Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problemsMelissa B Ramocki, Magdalena Bartnik, Przemyslaw Szafranski, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Overlapping spectra of SMAD4 mutations in juvenile polyposis (JP) and JP-HHT syndromeCarol Gallione, Arthur S Aylsworth, Jill Beis, et al.
American Journal of Human Genetics|October 11, 2011
Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorderMichael E Talkowski, Sureni V Mullegama, Jill A Rosenfeld, et al.
Pageof 4