Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

David T Miller

Showing results (71-80 of 107) with videos related to

Pageof 11
Sort By:
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 17, 2008
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypesZhishuo Ou, Jonathan S Berg, Hagith Yonath, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 22, 2023
ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Noura S Abul-Husn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 31, 2020
Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disordersSiddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2022
ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Noura S Abul-Husn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 12, 2019
Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disordersSiddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 26, 2025
ACMG SF v3.3 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)Kristy Lee, Noura S Abul-Husn, Laura M Amendola, et al.
Physiological Genomics|June 11, 2009
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing lossPu Dai, Andrew K Stewart, Fouad Chebib, et al.
Genes|April 8, 2020
Genomics of MPNST (GeM) Consortium: Rationale and Study Design for Multi-Omic Characterization of NF1-Associated and Sporadic MPNSTsDavid T Miller, Isidro Cortés-Ciriano, Nischalan Pillay, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2016
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and GenomicsSarah S Kalia, Kathy Adelman, Sherri J Bale, et al.
American Journal of Medical Genetics. Part A|July 4, 2007
Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogeneticsSau W Cheung, Chad A Shaw, Daryl A Scott, et al.
Pageof 11

Showing results (71-80 of 107) with videos related to

Sort By:
Pageof 11
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 17, 2008
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypesZhishuo Ou, Jonathan S Berg, Hagith Yonath, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 22, 2023
ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Noura S Abul-Husn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 31, 2020
Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disordersSiddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2022
ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Noura S Abul-Husn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 12, 2019
Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disordersSiddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 26, 2025
ACMG SF v3.3 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)Kristy Lee, Noura S Abul-Husn, Laura M Amendola, et al.
Physiological Genomics|June 11, 2009
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing lossPu Dai, Andrew K Stewart, Fouad Chebib, et al.
Genes|April 8, 2020
Genomics of MPNST (GeM) Consortium: Rationale and Study Design for Multi-Omic Characterization of NF1-Associated and Sporadic MPNSTsDavid T Miller, Isidro Cortés-Ciriano, Nischalan Pillay, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2016
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and GenomicsSarah S Kalia, Kathy Adelman, Sherri J Bale, et al.
American Journal of Medical Genetics. Part A|July 4, 2007
Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogeneticsSau W Cheung, Chad A Shaw, Daryl A Scott, et al.
Pageof 11