학술논문
Personalised virtual gene panels reduce interpretation workload and maintain diagnostic rates of proband-only clinical exome sequencing for rare disorders
Document Type
Journal
Author
Molina-Ramirez, Leslie Patricia; Kyle, Claire; Ellingford, Jamie M.; Wright, Ronnie; Taylor, Algy; Bhaskar, Sanjeev S.; Campbell, Christopher; Jackson, Harriet; Fairclough, Adele; Rousseau, Abigail; Burghel, George J.; Dutton, Laura; Banka, Siddharth; Briggs, Tracy A.; Clayton-Smith, Jill; Douzgou, Sofia; Jones, Elizabeth A.; Kingston, Helen M.; Kerr, Bronwyn; Ealing, John; Somarathi, Suresh; Chandler, Kate E.; Stuart, Helen M.; Burkitt-Wright, Emma M. M.; Newman, William G.; Bruce, Iain A.; Black, Graeme C.; Gokhale, David
Source
Subject
Language
English
ISSN
14686244