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Heidi L Rehm

Showing results (11-20 of 342) with videos related to

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Current Protocols in Human Genetics|April 23, 2008
Molecular diagnosis of hearing lossHeidi L Rehm
Ear and Hearing|August 19, 2003
Genetics and the genome projectHeidi L Rehm
Nature Medicine|February 8, 2022
Time to make rare disease diagnosis accessible to allHeidi L Rehm
JAMA Cardiology|March 1, 2018
Association of Racial/Ethnic Categories With the Ability of Genetic Tests to Detect a Cause of CardiomyopathyLatrice G Landry, Heidi L Rehm
Current Protocols in Human Genetics|January 14, 2012
Molecular diagnosis of hearing lossKerry K Brown, Heidi L Rehm
Nature|October 16, 2015
Building the foundation for genomics in precision medicineSamuel J Aronson, Heidi L Rehm
Journal of the National Cancer Institute|May 15, 2018
The Ancestral Pace of Variant ReclassificationSharon E Plon, Heidi L Rehm
American Journal of Human Genetics|December 12, 2023
Will variants of uncertain significance still exist in 2030?Douglas M Fowler, Heidi L Rehm
Lancet (London, England)|February 5, 2019
Introduction of genomics into prenatal diagnosticsMichael E Talkowski, Heidi L Rehm
Genome Medicine|November 23, 2019
Is 'likely pathogenic' really 90% likely? Reclassification data in ClinVarSteven M Harrison, Heidi L Rehm
Pageof 35

Showing results (11-20 of 342) with videos related to

Sort By:
Pageof 35
Current Protocols in Human Genetics|April 23, 2008
Molecular diagnosis of hearing lossHeidi L Rehm
Ear and Hearing|August 19, 2003
Genetics and the genome projectHeidi L Rehm
Nature Medicine|February 8, 2022
Time to make rare disease diagnosis accessible to allHeidi L Rehm
JAMA Cardiology|March 1, 2018
Association of Racial/Ethnic Categories With the Ability of Genetic Tests to Detect a Cause of CardiomyopathyLatrice G Landry, Heidi L Rehm
Current Protocols in Human Genetics|January 14, 2012
Molecular diagnosis of hearing lossKerry K Brown, Heidi L Rehm
Nature|October 16, 2015
Building the foundation for genomics in precision medicineSamuel J Aronson, Heidi L Rehm
Journal of the National Cancer Institute|May 15, 2018
The Ancestral Pace of Variant ReclassificationSharon E Plon, Heidi L Rehm
American Journal of Human Genetics|December 12, 2023
Will variants of uncertain significance still exist in 2030?Douglas M Fowler, Heidi L Rehm
Lancet (London, England)|February 5, 2019
Introduction of genomics into prenatal diagnosticsMichael E Talkowski, Heidi L Rehm
Genome Medicine|November 23, 2019
Is 'likely pathogenic' really 90% likely? Reclassification data in ClinVarSteven M Harrison, Heidi L Rehm
Pageof 35