Authors: Dahl, HHM Saunders, K Kelly, TM Osborn, AH Wilcox, S Cone-Wesson, B Wunderlich, JL Du Sart, D Kamarinos, M Gardner, RJM Dennehy, S Williamson, R Vallance, N Mutton, P

Citation: Hhm. Dahl et al., Prevalence and nature of connexin 26 mutations in children with non-syndromic deafness, MED J AUST, 175(4), 2001, pp. 191-194

Authors: Houseman, MJ Ellis, LA Pagnamenta, A Di, WL Rickard, S Osborn, AH Dahl, HHM Taylor, GR Bitner-Glindzicz, M Reardon, W Mueller, RF Kelsell, DP

Citation: Mj. Houseman et al., Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss, J MED GENET, 38(1), 2001, pp. 20-25

Authors: Wilcox, SA Osborn, AH Dahl, HHM

Citation: Sa. Wilcox et al., A simple PCR test to detect the common 35delG mutation in the connexin 26 gene, MOL DIAGN, 5(1), 2000, pp. 75-78

Authors: Wilcox, SA Saunders, K Osborn, AH Arnold, A Wunderlich, J Kelly, T Collins, V Wilcox, LJ Gardner, RJM Kamarinos, M Cone-Wesson, B Williamson, R Dahl, HHM

Citation: Sa. Wilcox et al., High frequency hearing loss correlated with mutations in the GJB2 gene, HUM GENET, 106(4), 2000, pp. 399-405

Authors: Dahl, HHM Osborn, AH Hutchison, WM Thorburn, DR Sheffield, LJ

Citation: Hhm. Dahl et al., Late diagnosis of maternal PKU in a family segregating an arylsulfatse E mutation causing symmetrical chondrodysplasia punctata, MOL GEN MET, 68(4), 1999, pp. 503-506

Authors: Wilcox, SA Osborn, AH Allen-Powell, DR Maw, MA Dahl, HHM Gardner, RJM

Citation: Sa. Wilcox et al., Connexin26 deafness in several interconnected families, J MED GENET, 36(5), 1999, pp. 383-385