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Journal of Personalized Medicine|July 27, 2022
Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive DiseasesEvgeniia A Sotnikova, Anna V Kiseleva, Vladimir A Kutsenko, et al.Genes|October 27, 2022
A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction CardiomyopathyRoman P Myasnikov, Olga V Kulikova, Alexey N Meshkov, et al.Frontiers in Cardiovascular Medicine|June 21, 2023
Genetic landscape in Russian patients with familial left ventricular noncompactionAlexey N Meshkov, Roman P Myasnikov, Anna V Kiseleva, et al.Gene|October 29, 2025
Cardiomyopathies, heart rhythm and conduction disorders as phenotypic manifestation of genetic variants in large cohort of cardiac patients: results of whole-genome studyElena M Rimskaya, Svetlana N Nasonova, Alexey N Meshkov, et al.Pageof 3