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Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert PanelMelissa A Kelly, Colleen Caleshu, Ana Morales, et al.Arthritis Research & Therapy|August 13, 2017
Lack of high BMI-related features in adipocytes and inflammatory cells in the infrapatellar fat pad (IFP)Anja J de Jong, Inge R Klein-Wieringa, Stefan N Andersen, et al.Nature Plants|December 10, 2020
The environmental impacts of palm oil in contextErik Meijaard, Thomas M Brooks, Kimberly M Carlson, et al.Human Mutation|October 13, 2018
Scaling resolution of variant classification differences in ClinVar between 41 clinical laboratories through an outlier approachSteven M Harrison, Jill S Dolinksy, Wenjie Chen, et al.The Journal of Molecular Diagnostics : JMD|February 25, 2021
Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM): A Study from the ClinGen Cardiomyopathy Variant Curation Expert PanelAna Morales, Alexander Ing, Christian Antolik, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 6, 2023
Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working GroupRyan J Schmidt, Marcie Steeves, Pinar Bayrak-Toydemir, et al.Circulation. Heart Failure|March 16, 2019
Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic CardiomyopathyVictoria N Parikh, Colleen Caleshu, Chloe Reuter, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2021
The genetic architecture of Plakophilin 2 cardiomyopathyAnnika M Dries, Anna Kirillova, Chloe M Reuter, et al.Pageof 9