Browsing by Author Hernandez-Hernandez, V
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Issue Date | Title | Author(s) |
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4-Feb-2014 | Loss of FTO Antagonises Wnt Signaling and Leads to Developmental Defects Associated with Ciliopathies | Osborn, DPS; Roccasecca, RM; McMurray, F; Hernandez-Hernandez, V; Mukherjee, S; Barroso, I; Stemple, D; Cox, R; Beales, PL; Christou-Savina, S |
2011 | Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome | Rooryck, C; Diaz-Font, A; Osborn, DPS; Chabchoub, E; Hernandez-Hernandez, V; Shamseldin, H; Kenny, J; Waters, A; Jenkins, D; Kaissi, AA; Leal, GF; Dallapiccola, B; Carnevale, F; Bitner-Glindzicz, M; Lees, M; Hennekam, R; Stanier, P; Burns, AJ; Peeters, H; Alkuraya, FS; Beales, PL |
1-Mar-2019 | Progressive Characterization of Visual Phenotype in Bardet-Biedl Syndrome Mutant MiceVisual Phenotype in Bardet-Biedl Syndrome Mice | Kretschmer, V; Patnaik, SR; Kretschmer, F; Chawda, MM; Hernandez-Hernandez, V; May-Simera, HL |