A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders
Titel:
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders
Auteur:
Simeoni, Ilenia Stephens, Jonathan C. Hu, Fengyuan Deevi, Sri V.V. Megy, Karyn Bariana, Tadbir K. Lentaigne, Claire Schulman, Sol Sivapalaratnam, Suthesh Vries, Minka J.A. Westbury, Sarah K. Greene, Daniel Papadia, Sofia Alessi, Marie-Christine Attwood, Antony P. Ballmaier, Matthias Baynam, Gareth Bermejo, Emilse Bertoli, Marta Bray, Paul F. Bury, Loredana Cattaneo, Marco Collins, Peter Daugherty, Louise C. Favier, Rémi French, Deborah L. Furie, Bruce Gattens, Michael Germeshausen, Manuela Ghevaert, Cedric Goodeve, Anne C. Guerrero, Jose A. Hampshire, Daniel J. Hart, Daniel P. Heemskerk, Johan W.M. Henskens, Yvonne M.C. Hill, Marian Hogg, Nancy Jolley, Jennifer D. Kahr, Walter H. Kelly, Anne M. Kerr, Ron Kostadima, Myrto Kunishima, Shinji Lambert, Michele P. Liesner, Ri López, José A. Mapeta, Rutendo P. Mathias, Mary Millar, Carolyn M. Nathwani, Amit Neerman-Arbez, Marguerite Nurden, Alan T. Nurden, Paquita Othman, Maha Peerlinck, Kathelijne Perry, David J. Poudel, Pawan Reitsma, Pieter Rondina, Matthew T. Smethurst, Peter A. Stevenson, William Szkotak, Artur Tuna, Salih van Geet, Christel Whitehorn, Deborah Wilcox, David A. Zhang, Bin Revel-Vilk, Shoshana Gresele, Paolo Bellissimo, Daniel B. Penkett, Christopher J. Laffan, Michael A. Mumford, Andrew D. Rendon, Augusto Gomez, Keith Freson, Kathleen Ouwehand, Willem H. Turro, Ernest