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Nature|February 18, 2026
Single-cell and isoform-specific translational profiling of the mouse brainSamantha L Sison, Federico Zampa, Eric R Kofman, et al.Human Molecular Genetics|December 27, 2011
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controlsRachel Soemedi, Ana Topf, Ian J Wilson, et al.Nature|November 25, 2021
A multi-scale map of cell structure fusing protein images and interactionsYue Qin, Edward L Huttlin, Casper F Winsnes, et al.American Journal of Human Genetics|September 4, 2012
Contribution of global rare copy-number variants to the risk of sporadic congenital heart diseaseRachel Soemedi, Ian J Wilson, Jamie Bentham, et al.Nature|July 31, 2020
A large-scale binding and functional map of human RNA-binding proteinsEric L Van Nostrand, Peter Freese, Gabriel A Pratt, et al.Heart, Lung & Circulation|November 19, 2019
Management of People With a Fontan Circulation: a Cardiac Society of Australia and New Zealand Position statementDominica Zentner, David S Celermajer, Thomas Gentles, et al.Genetics in Medicine Open|December 13, 2024
A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders FlagshipRachel Austin, Jaye S Brown, Sarah Casauria, et al.Circulation Research|December 10, 2021
Common Genetic Variants Contribute to Risk of Transposition of the Great ArteriesDoris Škorić-Milosavljević, Rafik Tadros, Fernanda M Bosada, et al.Pageof 17