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Whole-genome sequencing of patients with rare diseases in a national health system
Whole-genome sequencing of patients with rare diseases in a national health system
2021
Ernest Turro
William J. Astle
Karyn Megy
Stefan Gräf
Daniel Greene
Olga Shamardina
Hana Lango Allen
Alba Sanchis-Juan
Mattia Frontini
Chantal Thys
Jonathan Stephens
Rutendo Mapeta
Oliver S. Burren
Kate Downes
Matthias Haimel
Salih Tuna
Sri V.V. Deevi
Timothy J. Aitman
David Bennett
Paul Calleja
Keren J. Carss
Mark J. Caulfield
Patrick F. Chinnery
Peter H. Dixon
Daniel P. Gale
Roger James
Ania Koziell
Michael Laffan
Adam P. Levine
Eamonn R. Maher
Hugh S. Markus
Joannella Morales
Nicholas W. Morrell
Andrew D Mumford
Elizabeth Ormondroyd
Stuart Rankin
Augusto Rendon
Sylvia Richardson
Irene Roberts
Noemi B. A. Roy
Moin A. Saleem
Kenneth G. C. Smith
Hannah Stark
Rhea Y.Y. Tan
Andreas C. Themistocleous
Adrian J. Thrasher
Hugh Watkins
Andrew R. Webster
Martin R. Wilkins
Catherine Williamson
James Whitworth
Sean Humphray
David R. Bentley
Nathalie Kingston
Neil Walker
John Bradley
Sofie Ashford
Christopher J. Penkett
Kathleen Freson
Kathleen Stirrups
F. Lucy Raymond
Willem H. Ouwehand
Keywords:
Computational biology
Whole genome sequencing
national health
Medicine
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