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Whole-genome sequencing of patients with rare diseases in a national health system.

E. Turro, W. Astle, K. Megy, S. Gräf, D. Greene, O. Shamardina, H. Allen, A. Sanchis-Juan, M. Frontini, C. Thys, J. Stephens, R. Mapeta, O. Burren, K. Downes, M. Haimel, S. Tuna, S. Deevi, T. Aitman, D. Bennett, P. Calleja, K. Carss, M. Caulfield, P. Chinnery, P. Dixon, D. Gale, R. James, A. Koziell, M. Laffan, A. Levine, E. Maher, H. Markus, J. Morales, N. Morrell, A. Mumford, E. Ormondroyd, S. Rankin, A. Rendon, S. Richardson, I. Roberts, N. Roy, M. Saleem, K. Smith, H. Stark, R. Tan, A. Themistocleous, A. Thrasher, H. Watkins, A. Webster, M. Wilkins, C. Williamson, J. Whitworth, S. Humphray, D. Bentley, S. Abbs, L. Abulhoul, J. Adlard, M. Ahmed, H. Alachkar, D. Allsup, J. Almeida-King, P. Ancliff, R. Antrobus, R. Armstrong, G. Arno, S. Ashford, A. Attwood, P. Aurora, C. Babbs, C. Bacchelli, T. Bakchoul, S. Banka, T. Bariana, J. Barwell, J. Batista, H. Baxendale, P. Beales, A. Bierzynska, T. Biss, M. Bitner-Glindzicz, G. Black, M. Bleda, I. Blesneac, D. Bockenhauer, H. Bogaard, C. Bourne, S. Boyce, J. Bradley, E. Bragin, G. Breen, P. Brennan, C. Brewer, M. Brown, A. Browning, M. Browning, R. Buchan, M. Buckland, T. Bueser, C. Diz, J. Burn, S. Burns, N. Burrows, C. Campbell, G. Carr-White, R. Casey, J. Chambers, J. Chambers, M. Chan, C. Cheah, F. Cheng, M. Chitre, M. Christian, C. Church, J. Clayton-Smith, M. Cleary, N. Brod, G. Coghlan, E. Colby, T. Cole, J. Collins, P. Collins, C. Colombo, C. Compton, R. Condliffe, S. Cook, H. Cook, N. Cooper, P. Corris, A. Furnell, F. Cunningham, N. Curry, A. Cutler, M. Daniels, M. Dattani, L. Daugherty, J. Davis, A. Soyza, T. Dent, C. Deshpande, E. Dewhurst, S. Douzgou, A. Drazyk, E. Drewe, D. Duarte, T. Dutt, J. Edgar, K. Edwards, W. Egner, M. Ekani, P. Elliott, W. Erber, M. Erwood, M. Estiu, D. Evans, G. Evans, T. Everington, M. Eyries, H. Fassihi, R. Favier, J. Findhammer, D. Fletcher, F. Flinter, R. Floto, T. Fowler, J. Fox, A. Frary, C. French, K. Freson, H. Gall, V. Ganesan, M. Gattens, C. Geoghegan, T. Gerighty, A. Gharavi, S. Ghio, H. Ghofrani, J. Gibbs, K. Gibson, K. Gilmour, B. Girerd, N. Gleadall, S. Goddard, D. Goldstein, K. Gomez, P. Gordins, D. Gosal, J. Graham, L. Grassi, L. Greenhalgh, A. Greinacher, P. Gresele, P. Griffiths, S. Grigoriadou, R. Grocock, D. Grozeva, M. Gurnell, S. Hackett, C. Hadinnapola, W. Hague, R. Hague, M. Hall, H. Hanson, E. Haque, K. Harkness, A. Harper, C. Harris, D. Hart, A. Hassan, G. Hayman, A. Henderson, A. Herwadkar, J. Hoffman, S. Holden, R. Horvath, H. Houlden, A. Houweling, L. Howard, F. Hu, G. Hudson, J. Hughes, A. Huissoon, M. Humbert, S. Hunter, M. Hurles, M. Irving, L. Izatt, S. Johnson, S. Jolles, J. Jolley, D. Josifova, N. Jurkute, T. Karten, J. Karten, M. Kasanicki, H. Kazkaz, R. Kazmi, P. Kelleher, A. Kelly, W. Kelsall, C. Kempster, D. Kiely, N. Kingston, R. Klima, N. Koelling, M. Kostadima, G. Kovacs, R. Kreuzhuber, T. Kuijpers, A. Kumar, D. Kumararatne, M. Kurian, F. Lalloo, M. Lambert, A. Lawrie, D. Layton, N. Lench, C. Lentaigne, T. Lester, R. Linger, H. Longhurst, L. Lorenzo, E. Louka, P. Lyons, R. Machado, R. Ross, B. Madan, J. Maimaris, S. Malka, S. Mangles, K. Marchbank, S. Marks, H. Marschall, A. Marshall, J. Martin, M. Mathias, E. Matthews, H. Maxwell, P. McAlinden, M. McCarthy, H. McKinney, A. McMahon, S. Meacham, A. Mead, I. Castello, S. Mehta, M. Michaelides, C. Millar, S. Mohammed, S. Moledina, D. Montani, A. Moore, M. Mozere, K. Muir, A. Nemeth, W. Newman, M. Newnham, S. Noorani, P. Nurden, J. O'Sullivan, S. Obaji, C. Odhams, S. Okoli, A. Olschewski, H. Olschewski, K. Ong, S. Oram, W. Ouwehand, C. Palles, S. Papadia, S. Park, D. Parry, S. Patel, J. Paterson, A. Peacock, S. Pearce, J. Peden, K. Peerlinck, C. Penkett, J. Pepke-Zaba, R. Petersen, C. Pilkington, K. Poole, R. Prathalingam, B. Psaila, A. Pyle, R. Quinton, S. Rahman, A. Rao, F. Raymond, P. Rayner-Matthews, C. Rees, T. Renton, C. Rhodes, A. Rice, A. Richter, L. Robert, A. Rogers, S. Rose, R. Ross-Russell, C. Roughley, D. Ruddy, O. Sadeghi-Alavijeh, N. Samani, C. Samarghitean, R. Sargur, R. Sarkany, S. Satchell, S. Savic, J. Sayer, G. Sayer, L. Scelsi, A. Schaefer, S. Schulman, R. Scott, M. Scully, C. Searle, W. Seeger, A. Sen, W. Sewell, D. Seyres, N. Shah, S. Shapiro, A. Shaw, P. Short, K. Sibson, L. Side, I. Simeoni, M. Simpson, M. Sims, S. Sivapalaratnam, D. Smedley, K. Smith, K. Snape, N. Soranzo, F. Soubrier, L. Southgate, O. Spasic-Boskovic, S. Staines, E. Staples, C. Steward, K. Stirrups, A. Stuckey, J. Suntharalingam, E. Swietlik, P. Syrris, R. Tait, K. Talks, K. Tate, J. Taylor, J. Taylor, J. Thaventhiran, E. Thomas, D. Thomas, M. Thomas, P. Thomas, K. Thomson, G. Threadgold, T. Tilly, M. Tischkowitz, C. Titterton, J. Todd, C. Toh, B. Tolhuis, I. Tomlinson, M. Toshner, M. Traylor, C. Treacy, P. Treadaway, R. Trembath, W. Turek, P. Twiss, T. Vale, C. Geet, N. van Zuydam, M. Vandekuilen, A. Vandersteen, M. Vazquez-Lopez, J. von Ziegenweidt, A. Vonk-Noordegraaf, A. Wagner, Q. Waisfisz, S. Walker, N. Walker, K. Walter, J. Ware, C. Watt, L. Wedderburn, W. Wei, S. Welch, J. Wessels, S. Westbury, J. Westwood, J. Wharton, D. Whitehorn, A. Wilkie, B. Wilson, E. Wong, N. Wood, Y. Wood, C. Woods, E. Woodward, S. Wort, A. Worth, M. Wright, K. Yates, P. Yong, T. Young, P. Yu, P. Yu-Wai-Man, and E. Zlamalova. Nat., 583 (7814): 96-102 (2020)

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Sushila Gosalia

Alexander David

Helga Davidowa

Ellen David

Anita Maria Dávid

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Whole-genome sequencing of patients with rare diseases in a national health system.E. Turro, W. Astle, K. Megy, S. Gräf, D. Greene, O. Shamardina, H. Allen, A. Sanchis-Juan, M. Frontini, C. Thys and 439 other author(s). Nat., 583 (7814): 96-102 (2020)

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Disambiguation of "Gosal, David"

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Whole-genome sequencing of patients with rare diseases in a national health system.

Please choose a person to relate this publication to

Sushila Gosalia

Alexander David

Helga Davidowa

Ellen David

Anita Maria Dávid

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Gosal, David"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Whole-genome sequencing of patients with rare diseases in a national health system.

Please choose a person to relate this publication to

Sushila Gosalia

Alexander David

Helga Davidowa

Ellen David

Anita Maria Dávid

Other publications of authors with the same name

Disambiguation

copy delete add this publication to your clipboard
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URL
DOI
BibTeX
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APA
Chicago
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Whole-genome sequencing of patients with rare diseases in a national health system.