Showing 1 - 3 results of 3 for search 'Rainger, J', query time: 0.02s
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Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects. by Williamson, K, Rainger, J, Floyd, J, Ansari, M, Meynert, A, Aldridge, K, Rainger, J, Anderson, C, Moore, A, Hurles, M, Clarke, A, van Heyningen, V, Verloes, A, Taylor, MS, Wilkie, A, Fitzpatrick, DR
Published 2014Journal article -
2
Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations. by Rainger, J, Pehlivan, D, Johansson, S, Bengani, H, Sanchez-Pulido, L, Williamson, K, Ture, M, Barker, H, Rosendahl, K, Spranger, J, Horn, D, Meynert, A, Floyd, J, Prescott, T, Anderson, C, Rainger, J, Karaca, E, Gonzaga-Jauregui, C, Jhangiani, S, Muzny, D, Seawright, A, Soares, D, Kharbanda, M, Murday, V, Finch, A
Published 2014Journal article -
3
Arginine to glutamine mutation in olfactomedin-like 3 (OLFML3) is a candidate for severe goniodysgenesis and glaucoma in the Border Collie dog breed by Pugh, C, Farrell, L, Carlisle, A, Bush, S, Trejo-Reveles, V, Matika, O, De Kloet, A, Walsh, C, Bishop, S, Prendergast, J, Schoenebeck, J, Rainger, J, Summers, K
Published 2019Journal article