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E Prescott

Showing results (161-170 of 181) with videos related to

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European Journal of Medical Genetics|June 12, 2016
Two male sibs with severe micrognathia and a missense variant in MED12Trine E Prescott, Mari Ann Kulseth, Ketil R Heimdal, et al.
The Journal of General Virology|July 28, 1999
Sequence diversity of TT virus in geographically dispersed human populationsL E Prescott, D M MacDonald, F Davidson, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|January 13, 2025
Molecular Determinants of Protein Pathogenicity at the Single-Aggregate LevelAgnieszka Urbanek, Emma F Garland, Emily E Prescott, et al.
International Journal of Cardiology|August 22, 2021
EU-CaRE study: Could exercise-based cardiac telerehabilitation also be cost-effective in elderly?M Scherrenberg, U Zeymer, S Schneider, et al.
The Cochrane Database of Systematic Reviews|October 28, 2021
Phototherapy for atopic eczemaAnnelie H Musters, Soudeh Mashayekhi, Jane Harvey, et al.
Molecular Syndromology|April 10, 2014
Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studiesA M Zink, E Wohlleber, H Engels, et al.
American Journal of Human Genetics|October 10, 2007
Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone developmentM A Simpson, R Hsu, L S Keir, et al.
Journal of Medical Genetics|December 5, 2023
Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridiaHildegard Nikki Hall, David Parry, Mihail Halachev, et al.
Dysphagia|March 7, 1998
Comparing treatment intensities of tactile-thermal applicationJ C Rosenbek, J Robbins, W O Willford, et al.
American Journal of Human Genetics|December 29, 2015
Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual DisabilityAsbjørg Stray-Pedersen, Jan-Maarten Cobben, Trine E Prescott, et al.
Pageof 19

Showing results (161-170 of 181) with videos related to

Sort By:
Pageof 19
European Journal of Medical Genetics|June 12, 2016
Two male sibs with severe micrognathia and a missense variant in MED12Trine E Prescott, Mari Ann Kulseth, Ketil R Heimdal, et al.
The Journal of General Virology|July 28, 1999
Sequence diversity of TT virus in geographically dispersed human populationsL E Prescott, D M MacDonald, F Davidson, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|January 13, 2025
Molecular Determinants of Protein Pathogenicity at the Single-Aggregate LevelAgnieszka Urbanek, Emma F Garland, Emily E Prescott, et al.
International Journal of Cardiology|August 22, 2021
EU-CaRE study: Could exercise-based cardiac telerehabilitation also be cost-effective in elderly?M Scherrenberg, U Zeymer, S Schneider, et al.
The Cochrane Database of Systematic Reviews|October 28, 2021
Phototherapy for atopic eczemaAnnelie H Musters, Soudeh Mashayekhi, Jane Harvey, et al.
Molecular Syndromology|April 10, 2014
Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studiesA M Zink, E Wohlleber, H Engels, et al.
American Journal of Human Genetics|October 10, 2007
Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone developmentM A Simpson, R Hsu, L S Keir, et al.
Journal of Medical Genetics|December 5, 2023
Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridiaHildegard Nikki Hall, David Parry, Mihail Halachev, et al.
Dysphagia|March 7, 1998
Comparing treatment intensities of tactile-thermal applicationJ C Rosenbek, J Robbins, W O Willford, et al.
American Journal of Human Genetics|December 29, 2015
Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual DisabilityAsbjørg Stray-Pedersen, Jan-Maarten Cobben, Trine E Prescott, et al.
Pageof 19