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Heidi L Rehm

Showing results (51-60 of 342) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2023
Multilevel barriers and facilitators to widespread use of preconception carrier screening in the United StatesLeland E Hull, Kelsey Flannery, Anjali Kaimal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 28, 2022
Importance of adopting standardized MANE transcripts in clinical reportingCaroline F Wright, David R FitzPatrick, James S Ware, et al.
Prenatal Diagnosis|March 28, 2017
Prenatal DNA Sequencing: Clinical, Counseling, and Diagnostic Laboratory ConsiderationsAhmad N Abou Tayoun, Nancy B Spinner, Heidi L Rehm, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 10, 2021
An Investigation of the Knowledge Overlap between Pharmacogenomics and Disease GeneticsBinglan Li, Michelle Whirl-Carrillo, Matt W Wright, et al.
Nature Genetics|June 2, 2023
Tracking genetic variants in the biomedical literature using LitVar 2.0Alexis Allot, Chih-Hsuan Wei, Lon Phan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2012
Communicating new knowledge on previously reported genetic variantsSamuel J Aronson, Eugene H Clark, Matthew Varugheese, et al.
JAMA|October 22, 2009
Implications of hypertrophic cardiomyopathy transmitted by sperm donationBarry J Maron, John R Lesser, Nelson B Schiller, et al.
Healthcare (Basel, Switzerland)|December 22, 2023
A Panel-Agnostic Strategy 'HiPPo' Improves Diagnostic Efficiency in the UK Genomic Medicine ServiceEleanor G Seaby, N Simon Thomas, David Hunt, et al.
Nature Reviews. Nephrology|April 9, 2020
Diagnoses of uncertain significance: kidney genetics in the 21st centuryDaniel P Gale, Andrew Mallett, Chirag Patel, et al.
American Journal of Human Genetics|July 4, 2020
Management of Secondary Genomic FindingsAlexander E Katz, Robert L Nussbaum, Benjamin D Solomon, et al.
Pageof 35

Showing results (51-60 of 342) with videos related to

Sort By:
Pageof 35
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2023
Multilevel barriers and facilitators to widespread use of preconception carrier screening in the United StatesLeland E Hull, Kelsey Flannery, Anjali Kaimal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 28, 2022
Importance of adopting standardized MANE transcripts in clinical reportingCaroline F Wright, David R FitzPatrick, James S Ware, et al.
Prenatal Diagnosis|March 28, 2017
Prenatal DNA Sequencing: Clinical, Counseling, and Diagnostic Laboratory ConsiderationsAhmad N Abou Tayoun, Nancy B Spinner, Heidi L Rehm, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 10, 2021
An Investigation of the Knowledge Overlap between Pharmacogenomics and Disease GeneticsBinglan Li, Michelle Whirl-Carrillo, Matt W Wright, et al.
Nature Genetics|June 2, 2023
Tracking genetic variants in the biomedical literature using LitVar 2.0Alexis Allot, Chih-Hsuan Wei, Lon Phan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2012
Communicating new knowledge on previously reported genetic variantsSamuel J Aronson, Eugene H Clark, Matthew Varugheese, et al.
JAMA|October 22, 2009
Implications of hypertrophic cardiomyopathy transmitted by sperm donationBarry J Maron, John R Lesser, Nelson B Schiller, et al.
Healthcare (Basel, Switzerland)|December 22, 2023
A Panel-Agnostic Strategy 'HiPPo' Improves Diagnostic Efficiency in the UK Genomic Medicine ServiceEleanor G Seaby, N Simon Thomas, David Hunt, et al.
Nature Reviews. Nephrology|April 9, 2020
Diagnoses of uncertain significance: kidney genetics in the 21st centuryDaniel P Gale, Andrew Mallett, Chirag Patel, et al.
American Journal of Human Genetics|July 4, 2020
Management of Secondary Genomic FindingsAlexander E Katz, Robert L Nussbaum, Benjamin D Solomon, et al.
Pageof 35