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Nucleic Acids Research|April 16, 2008
DNA bar coding and pyrosequencing to analyze adverse events in therapeutic gene transferGary P Wang, Alexandrine Garrigue, Angela Ciuffi, et al.
Plos Pathogens|June 23, 2006
Retroviral DNA integration: viral and cellular determinants of target-site selectionMary K Lewinski, Masahiro Yamashita, Michael Emerman, et al.
Cell Metabolism|September 4, 2018
Mitochondrial DNA Variation Dictates Expressivity and Progression of Nuclear DNA Mutations Causing CardiomyopathyMeagan J McManus, Martin Picard, Hsiao-Wen Chen, et al.
Human Mutation|February 27, 2016
MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial DiseaseLishuang Shen, Maria Angela Diroma, Michael Gonzalez, et al.
American Journal of Human Genetics|December 6, 2024
Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trialStephen F Kingsmore, Meredith Wright, Lauren Olsen, et al.
American Journal of Human Genetics|December 6, 2024
Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselectionStephen F Kingsmore, Meredith Wright, Laurie D Smith, et al.
Nature|May 14, 2013
De novo mutations in histone-modifying genes in congenital heart diseaseSamir Zaidi, Murim Choi, Hiroko Wakimoto, et al.
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