Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia

Nikki Hall, David A. Parry, Mihail Halachev, Kathy Williamson, Kevin Donnelly, Jose Campos Parada, Shipra Bhatia, Jeffrey Joseph, Simon Holden, Trine E Prescott, Pierre Bitoun, Edwin Kirk, Ruth Newbury-Ecob, Katherine Lachlan, Juan Bernar, Veronica Van Heyningen, David R FitzPatrick, Alison M Meynert*

*Corresponding author for this work

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