Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia
Hall, Hildegard Nikki, Parry, David, Halachev, Mihail, Williamson, Kathleen A, Donnelly, Kevin, Campos Parada, Jose, Bhatia, Shipra, Joseph, Jeffrey, Holden, Simon, Prescott, Trine E, Bitoun, Pierre, Kirk, Edwin P, Newbury-Ecob, Ruth, Lachlan, Katherine, Bernar, Juan, van Heyningen, Veronica, FitzPatrick, David R, Meynert, Alison
Published in Journal of medical genetics (01.03.2024)
Published in Journal of medical genetics (01.03.2024)
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