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Showing results (251-260 of 475) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 13, 2018
Health behaviors among unaffected participants following receipt of variants of uncertain significance in cardiomyopathy-associated genesIlana M Miller, Katie L Lewis, Tokunbor A Lawal, et al.
Scientific Reports|March 23, 2021
Cardiothoracic imaging findings of Proteus syndromeS Mojdeh Mirmomen, Andrew E Arai, Evrim B Turkbey, et al.
Human Mutation|September 8, 2018
Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterionAhmad N Abou Tayoun, Tina Pesaran, Marina T DiStefano, et al.
Public Health Genomics|August 6, 2023
Genetic Testing and Other Healthcare Use by Black and White Individuals in a Genomic Sequencing StudyKatherine W Saylor, William M P Klein, Larissa Calancie, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|February 11, 2020
Acute Statin Administration Reduces Levels of Steroid Hormone PrecursorsEdra London, Christina Tatsi, Steven J Soldin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 27, 2021
Evaluating the impact of in silico predictors on clinical variant classificationEmma H Wilcox, Mahdi Sarmady, Bryan Wulf, et al.
European Journal of Human Genetics : EJHG|August 16, 2012
Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq studyFlavia M Facio, Haley Eidem, Tyler Fisher, et al.
Orphanet Journal of Rare Diseases|February 6, 2024
Quantification of Proteus syndrome-associated lung diseaseChristopher A Ours, Anna Buser, Mia B Hodges, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 5, 2011
The pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signalingDerek E Gildea, Erin S Luetkemeier, Xiaozhong Bao, et al.
Human Molecular Genetics|April 7, 2025
Calibrating a functional assay for variant classification in RYR1-related malignant hyperthermia susceptibilityEvan Z Ying, Amber Douglass, Marwan A Hawari, et al.
Pageof 48

Showing results (251-260 of 475) with videos related to

Sort By:
Pageof 48
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 13, 2018
Health behaviors among unaffected participants following receipt of variants of uncertain significance in cardiomyopathy-associated genesIlana M Miller, Katie L Lewis, Tokunbor A Lawal, et al.
Scientific Reports|March 23, 2021
Cardiothoracic imaging findings of Proteus syndromeS Mojdeh Mirmomen, Andrew E Arai, Evrim B Turkbey, et al.
Human Mutation|September 8, 2018
Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterionAhmad N Abou Tayoun, Tina Pesaran, Marina T DiStefano, et al.
Public Health Genomics|August 6, 2023
Genetic Testing and Other Healthcare Use by Black and White Individuals in a Genomic Sequencing StudyKatherine W Saylor, William M P Klein, Larissa Calancie, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|February 11, 2020
Acute Statin Administration Reduces Levels of Steroid Hormone PrecursorsEdra London, Christina Tatsi, Steven J Soldin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 27, 2021
Evaluating the impact of in silico predictors on clinical variant classificationEmma H Wilcox, Mahdi Sarmady, Bryan Wulf, et al.
European Journal of Human Genetics : EJHG|August 16, 2012
Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq studyFlavia M Facio, Haley Eidem, Tyler Fisher, et al.
Orphanet Journal of Rare Diseases|February 6, 2024
Quantification of Proteus syndrome-associated lung diseaseChristopher A Ours, Anna Buser, Mia B Hodges, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 5, 2011
The pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signalingDerek E Gildea, Erin S Luetkemeier, Xiaozhong Bao, et al.
Human Molecular Genetics|April 7, 2025
Calibrating a functional assay for variant classification in RYR1-related malignant hyperthermia susceptibilityEvan Z Ying, Amber Douglass, Marwan A Hawari, et al.
Pageof 48