Optimizing the Diagnosis of Rare Genomic Disease in the UK and Ireland

Authors :: Wright, Caroline F
Campbell, Patrick
Eberhardt, Ruth Y.
Aitken, Stuart
Perrett, Daniel
Brent, Simon
Danecek, Petr
Gardner, Eugene J.
Chundru, V Kartik
Lindsay, Sarah J
Andrews, Katrina A
Hampstead, Juliet
Kaplanis, Joanna
Samocha, Kaitlin E.
Middleton, Anna
Foreman, Julia
Hobson, Rachel J.
Parker, Michael J.
Martin, Hilary C
FitzPatrick, David R
Hurles, Matthew E
Firth, Helen V.
Source :: Wright, C F, Campbell, P, Eberhardt, R Y, Aitken, S, Perrett, D, Brent, S, Danecek, P, Gardner, E J, Chundru, V K, Lindsay, S J, Andrews, K A, Hampstead, J, Kaplanis, J, Samocha, K E, Middleton, A, Foreman, J, Hobson, R J, Parker, M J, Martin, H C, FitzPatrick, D R, Hurles, M E & Firth, H V 2023, ' Optimizing the Diagnosis of Rare Genomic Disease in the UK and Ireland ', New England Journal of Medicine .
Publication Year :: 2023

Language :: English
Database :: OpenAIRE
Journal :: Wright, C F, Campbell, P, Eberhardt, R Y, Aitken, S, Perrett, D, Brent, S, Danecek, P, Gardner, E J, Chundru, V K, Lindsay, S J, Andrews, K A, Hampstead, J, Kaplanis, J, Samocha, K E, Middleton, A, Foreman, J, Hobson, R J, Parker, M J, Martin, H C, FitzPatrick, D R, Hurles, M E & Firth, H V 2023, ' Optimizing the Diagnosis of Rare Genomic Disease in the UK and Ireland ', New England Journal of Medicine .
Accession number :: edsair.od......3094..82a946077b9d08839b0fbf99e61deb33

Tools