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

Heidi L Rehm

Showing results (21-30 of 342) with videos related to

Pageof 35
Sort By:
Genome Medicine|November 23, 2019
Is 'likely pathogenic' really 90% likely? Reclassification data in ClinVarSteven M Harrison, Heidi L Rehm
The New England Journal of Medicine|October 3, 2015
ClinGen and Genetic TestingRobert L Nussbaum, Heidi L Rehm,
JAMA|April 11, 2013
New approaches to molecular diagnosisBruce R Korf, Heidi L Rehm
Biorxiv : the Preprint Server for Biology|May 22, 2023
Insights from a genome-wide truth set of tandem repeat variationBen Weisburd, Grace Tiao, Heidi L Rehm
Genome Medicine|December 29, 2020
Genetic variation in the Middle East-an opportunity to advance the human genetics fieldAhmad N Abou Tayoun, Heidi L Rehm
Ear and Hearing|August 19, 2003
Glossary for hereditary hearing impairmentMarkus H F Pfister, Heidi L Rehm
Journal of Personalized Medicine|February 2, 2016
The Changing Landscape of Molecular Diagnostic Testing: Implications for Academic Medical CentersHeidi L Rehm, Elizabeth Hynes, Birgit H Funke
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 6, 2020
Correspondence on "The role of clinical response to treatment in determining pathogenicity of genomic variants" by Shen et alLeslie G Biesecker, Steven M Harrison, Heidi L Rehm
Mayo Clinic Proceedings|August 26, 2023
An Environmental Scan of Consumer-Initiated Germline Genetic Testing for Health RisksHannah G Kirby, Heidi L Rehm, Leland E Hull
Current Protocols in Human Genetics|September 4, 2019
Overview of Specifications to the ACMG/AMP Variant Interpretation GuidelinesSteven M Harrison, Leslie G Biesecker, Heidi L Rehm
Pageof 35

Showing results (21-30 of 342) with videos related to

Sort By:
Pageof 35
Genome Medicine|November 23, 2019
Is 'likely pathogenic' really 90% likely? Reclassification data in ClinVarSteven M Harrison, Heidi L Rehm
The New England Journal of Medicine|October 3, 2015
ClinGen and Genetic TestingRobert L Nussbaum, Heidi L Rehm,
JAMA|April 11, 2013
New approaches to molecular diagnosisBruce R Korf, Heidi L Rehm
Biorxiv : the Preprint Server for Biology|May 22, 2023
Insights from a genome-wide truth set of tandem repeat variationBen Weisburd, Grace Tiao, Heidi L Rehm
Genome Medicine|December 29, 2020
Genetic variation in the Middle East-an opportunity to advance the human genetics fieldAhmad N Abou Tayoun, Heidi L Rehm
Ear and Hearing|August 19, 2003
Glossary for hereditary hearing impairmentMarkus H F Pfister, Heidi L Rehm
Journal of Personalized Medicine|February 2, 2016
The Changing Landscape of Molecular Diagnostic Testing: Implications for Academic Medical CentersHeidi L Rehm, Elizabeth Hynes, Birgit H Funke
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 6, 2020
Correspondence on "The role of clinical response to treatment in determining pathogenicity of genomic variants" by Shen et alLeslie G Biesecker, Steven M Harrison, Heidi L Rehm
Mayo Clinic Proceedings|August 26, 2023
An Environmental Scan of Consumer-Initiated Germline Genetic Testing for Health RisksHannah G Kirby, Heidi L Rehm, Leland E Hull
Current Protocols in Human Genetics|September 4, 2019
Overview of Specifications to the ACMG/AMP Variant Interpretation GuidelinesSteven M Harrison, Leslie G Biesecker, Heidi L Rehm
Pageof 35