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Heidi L Rehm

Showing results (171-180 of 342) with videos related to

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Human Mutation|March 25, 2011
The GeneInsight Suite: a platform to support laboratory and provider use of DNA-based genetic testingSamuel J Aronson, Eugene H Clark, Lawrence J Babb, et al.
Circulation. Genomic and Precision Medicine|March 12, 2020
Variant Interpretation for Dilated Cardiomyopathy: Refinement of the American College of Medical Genetics and Genomics/ClinGen Guidelines for the DCM Precision Medicine StudyAna Morales, Daniel D Kinnamon, Elizabeth Jordan, et al.
European Journal of Human Genetics : EJHG|November 10, 2020
Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
European Journal of Human Genetics : EJHG|December 13, 2019
Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
Med (New York, N.Y.)|May 19, 2022
JAK inhibition in a patient with a STAT1 gain-of-function variant reveals STAT1 dysregulation as a common feature of aplastic anemiaJacob M Rosenberg, Joshua M Peters, Travis Hughes, et al.
Genome Research|January 25, 2022
Mitochondrial DNA variation across 56,434 individuals in gnomADKristen M Laricchia, Nicole J Lake, Nicholas A Watts, et al.
American Journal of Human Genetics|August 20, 2019
Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical SettingAdam S Gordon, Elisabeth A Rosenthal, David S Carrell, et al.
Investigative Ophthalmology & Visual Science|August 30, 2011
Retinal disease course in Usher syndrome 1B due to MYO7A mutationsSamuel G Jacobson, Artur V Cideciyan, Dan Gibbs, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 8, 2014
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencingTrevor J Pugh, Melissa A Kelly, Sivakumar Gowrisankar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 26, 2021
Universal newborn genetic screening for pediatric cancer predisposition syndromes: model-based insightsJennifer M Yeh, Natasha K Stout, Aeysha Chaudhry, et al.
Pageof 35

Showing results (171-180 of 342) with videos related to

Sort By:
Pageof 35
Human Mutation|March 25, 2011
The GeneInsight Suite: a platform to support laboratory and provider use of DNA-based genetic testingSamuel J Aronson, Eugene H Clark, Lawrence J Babb, et al.
Circulation. Genomic and Precision Medicine|March 12, 2020
Variant Interpretation for Dilated Cardiomyopathy: Refinement of the American College of Medical Genetics and Genomics/ClinGen Guidelines for the DCM Precision Medicine StudyAna Morales, Daniel D Kinnamon, Elizabeth Jordan, et al.
European Journal of Human Genetics : EJHG|November 10, 2020
Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
European Journal of Human Genetics : EJHG|December 13, 2019
Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
Med (New York, N.Y.)|May 19, 2022
JAK inhibition in a patient with a STAT1 gain-of-function variant reveals STAT1 dysregulation as a common feature of aplastic anemiaJacob M Rosenberg, Joshua M Peters, Travis Hughes, et al.
Genome Research|January 25, 2022
Mitochondrial DNA variation across 56,434 individuals in gnomADKristen M Laricchia, Nicole J Lake, Nicholas A Watts, et al.
American Journal of Human Genetics|August 20, 2019
Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical SettingAdam S Gordon, Elisabeth A Rosenthal, David S Carrell, et al.
Investigative Ophthalmology & Visual Science|August 30, 2011
Retinal disease course in Usher syndrome 1B due to MYO7A mutationsSamuel G Jacobson, Artur V Cideciyan, Dan Gibbs, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 8, 2014
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencingTrevor J Pugh, Melissa A Kelly, Sivakumar Gowrisankar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 26, 2021
Universal newborn genetic screening for pediatric cancer predisposition syndromes: model-based insightsJennifer M Yeh, Natasha K Stout, Aeysha Chaudhry, et al.
Pageof 35