Items where Division is "Faculties (pre 2018 reorg) > Faculty of Medicine (pre 2018 reorg) > Human Development & Health (pre 2018 reorg) > Human Genetics (pre 2018 reorg)
Current Faculties > Faculty of Medicine > Human Development and Health > Human Development & Health (pre 2018 reorg) > Human Genetics (pre 2018 reorg)
Human Development and Health > Human Development & Health (pre 2018 reorg) > Human Genetics (pre 2018 reorg)" and Year is 2019
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Number of items: 3.
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PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age related clonal hermatopoiesis and myeloid neoplasia - Andrew Chase, Andrea Pellagatti, Shalini Singh, Joannah Score, William J. Tapper, Feng Lin, Yvette M. Hoade, Catherine Bryant, Nicola Trim, Bon Ham Yip, Katerina Zoi, Chiara Rasi, Lars A. Forsberg, Jan P. Dumanski, Jacqueline Boultwood and Nicholas C.P. Cross
Type: Article
| 2019
Recurrent activating STAT5B N642H mutation in myeloid neoplasms with eosinophilia - Nicholas Cross, Yvette Hoade, William Tapper, Gonzalo Carreno-Tarragona, Tiziana Fanelli, Mohamad Jawhar, Nicole Naumann, Iwo Pieniak, Johannes Lübke, Sahra Ali, Kaljit Bhuller, Sonja Burgstaller, Catherine Cargo, Jamie Cavenagh, Andrew S. Duncombe, Emma Das-Gupta, Paul Evans, Peter Forsyth, Philip George, Charlotte Grimley, Fergus Jack, Laura Munro, Varun Mehra, Kavita Patel, Ali Rismani, Gabriela Sciuccati, Rowena Thomas-Dewing, Patrick Thornton, Andres Virchis, Simon Watt, Louise Wallis, Alistair Whiteway, Kris Zegocki, Barbara J. Bain, Andreas Reiter and Andrew Chase
Type: Article
| 2019
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Understanding the disease genome: gene essentiality and the interplay of selection, recombination and mutation - Reuben J. Pengelly, Alejandra Vergara Lope, Dareen Alyousfi, M. Reza Jabalameli and Andrew Collins
Type: Article
| 2019