학술논문

Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants
Document Type
Article
Author
Bournazos, A.M.Bommireddipalli, S.Bryen, S.J.Dawes, R.Joshi, H.Lemckert, F.Sandaradura, S.A.Wong, W.K.Jones, K.J.Cooper, S.T.Riley, L.G.Ades, L.Alexander, S.I.Ho, G.Ma, A.McCarthy, H.J.Menezes, M.P.Mohammad, S.Tantsis, E.Wright, D.C.Bennetts, B.Niaz, A.Boggs, K.Josephi-Taylor, S.Samarasekera, R.Shah, M.Smith, J.M.Wilson, M.J.Akesson, L.S.Archibald, A.D.Brown, N.J.Delatycki, M.Downie, L.Fennell, A.Gallacher, L.Horton, A.E.Leventer, R.J.Stark, Z.Tan, T.Y.White, S.M.Yeung, A.Huq, A.J.Trainer, A.H.Lunke, S.Chong, B.Gear, R.Marty, M.Marum, J.E.Phelan, D.Savva, E.Beshay, V.Macaskill, S.Al-Shinnag, M.Higgins, M.Milnes, D.Patel, C.Rodgers, J.van Spaendonck-Zwarts, K.Balasubramaniam, S.Sinnerbrink, I.B.Tchan, M.C.Berman, Y.White, S.Bojadzieva, J.Buckley, M.F.Kirk, E.Roscioli, T.Walsh, R.Davis, M.R.Edwards, C.Faiz, F.Donaldson, L.Edwards, M.Engel, A.Warwick, L.Ewans, L.J.Mallawaarachchi, A.Hunter, M.F.Krzesinski, E.Regan, M.Field, M.Goel, H.Freckmann, M.-L.Goh, S.Lindsey-Temple, S.E.McLean, A.Rajagopalan, S.Goodwin, L.Hanna, B.Harraway, J.Hopper, B.K.Springer, A.Tan, K.Mowat, D.Palmer, E.E.Pinner, J.R.Sachdev, R.Kumar, K.R.Sue, C.M.Schindler, T.Patel, S.G.Rodrigues, M.Roxburgh, R.H.Smith, R.J.Strom, S.P.Thompson, B.A.Williams, M.G.Yap, P.Young, H.Abdulrasool, G.Al Eryani, G.Arts, P.Bagnall, R.Baker, N.L.Barnett, C.Beecroft, S.Berbic, M.Black, M.Blackburn, J.Blombery, P.Branford, S.Breen, J.Burnett, L.Canson, D.Cheong, P.Chew, E.Christodoulou, J.Chung, S.-K.Clark, M.Cliffe, C.Cole, M.Collins, F.Compton, A.Cooper, A.Corbett, M.Cowley, M.Dudding, T.Eggers, S.Eyras, E.Fernandez, M.F.Fellowes, A.Fleischer, R.Folland, C.Fox, L.Gaff, C.Galea, M.Ghaoui, R.Gornanitis, I.Ha, T.Hayashi, R.Hayes, I.Henderson, A.Hesson, L.Heyer, E.Hildebrand, M.Hipwell, M.Hoskins, C.Jackson, M.James, P.Wong, J.J.-L.Kassahn, K.Kaub, P.Kevin, L.Kumble, S.Kummerfeld, S.Laing, N.Lau, C.Lee, E.Leighton, S.Lundie, B.Mayoh, C.McGaughran, J.McPhillips, M.Meldrum, C.Middleton, E.Mina, K.Nisselle, A.Oates, E.Oshlack, A.Parasivam, G.Parsons, M.Quinn, M.Rasko, J.Ravenscroft, G.Ravine, A.Recsei, K.Rehn, J.Robertson, S.Ronan, A.Ryland, G.Sadedin, S.Schreiber, A.Scott, H.Scott, R.Semsarian, C.Simons, C.Singer, E.Smyth, R.Spurdle, A.Sullivan, P.Sundercombe, S.Thorburn, D.Toubia, J.Trent, R.Tudini, E.Voneague, I.Waddell, L.Walker, L.Wallis, M.Warnock, N.Weatheritt, R.White, D.Winship, I.Worgan, L.Wu, K.Ziolowski, A.
Source
In: Genetics in Medicine. (Genetics in Medicine, January 2022, 24(1):130-145)
Subject
Language
English
ISSN
15300366
10983600