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whole exome sequencing
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Whole Exome Sequencing
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clinical article
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gene mutation
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high throughput sequencing
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single nucleotide polymorphism
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genetic analysis
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genetic variability
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1by Birkeland, A.C, Brenner, J.C, Carey, T.E, Devenport, S.N, Foltin, S.K, Hoesli, R.C, Jewell, B.M, Jiang, H., Kulkarni, A., Ludwig, M.L, Mann, J.E, Michmerhuizen, N.L, Shuman, A.G, Spector, M.EView Fulltext in Publisher
Published 2018
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14by Akesson, L.S, Amarasekera, S., Bordador, E., Brown, N.J, Chai, C., Chong, B., Christodoulou, J., Compton, A.G, Donoghue, S., Guo, Y., Hakonarson, H., Lee, C., Lunke, S., Marum, J., Monaco, A., Rius, R., Rosenbaum, J., Stark, Z., Stormon, M., Thorburn, D.RView Fulltext in Publisher
Published 2022
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20by Akhter, A., Bhalla, K., Bouska, A., Buckley, S., Carey, C., Chen, B.J, Davidson, M., Davis, R.E, Deng, Q., Fowler, N.H, Gandhi, M., Ghosh, S., Green, M.R, Greiner, T., Hartert, K., Heavican, T., Iqbal, J., Jain, N., Lunning, M.A, Ma, M.C.J, Mansoor, A., Moore, D., Nastoupil, L.J, Neelapu, S., Parekh, S., Perumal, D., Rodig, S.J, Showell, J., Sohani, A.R, Stewart, D., Street, L., Tadros, S., Tobin, J., Vose, J.M, Westin, J.R, Yang, H.View Fulltext in Publisher
Published 2022
Article