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American Journal of Human Genetics|September 6, 2024
Implementation of a dyadic nomenclature for monogenic diseasesCourtney Thaxton, Leslie G Biesecker, Marina DiStefano, et al.
Cell Genomics|June 27, 2022
Lumping versus splitting: How to approach defining a disease to enable accurate genomic curationCourtney Thaxton, Jennifer Goldstein, Marina DiStefano, et al.
Physiology & Behavior|December 17, 2025
Gastrointestinal dysmotility and impaired gut peptide-satiety coupling in men with spinal cord injuryGary J Farkas, Paige M Cunningham, Arthur S Berg, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|March 1, 1997
Heritability for Alzheimer's disease: the study of dementia in Swedish twinsM Gatz, N L Pedersen, S Berg, et al.
MDM Policy & Practice|June 22, 2018
Development and Validation of a Genomic Knowledge Scale to Advance Informed Decision Making Research in Genomic SequencingMichelle M Langer, Myra I Roche, Noel T Brewer, et al.
Prenatal Diagnosis|July 15, 2021
Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fractionDayne L Filer, Piotr A Mieczkowski, Alicia Brandt, et al.
Pediatrics|January 6, 2016
Supporting Parental Decisions About Genomic Sequencing for Newborn Screening: The NC NEXUS Decision AidMegan A Lewis, Ryan S Paquin, Myra I Roche, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 28, 2019
Expert and lay perspectives on burden, risk, tolerability, and acceptability of clinical interventions for genetic disordersRyan S Paquin, Kathleen F Mittendorf, Megan A Lewis, et al.
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