Access to Sexual Health Services and Support for People with Intellectual and Developmental Disabilities: an Australian Cross-sector Survey

por Frawley, Patsie, Wilson, N.J., David, Jennifer, O’Shea, Amie, Areskoug Josefsson, K.
Publicado 2022

Isolated recessive nail dysplasia caused by FZD6 mutations: report of three families and review of the literature

por Kasparis, C., Reid, D., Wilson, N. J., Okur, V., Cole, C., Hansen, C. D., Bosse, K., Betz, R. C., Khan, M., Smith, F. J. D.
Publicado 2016

Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening

por Lovgren, M.‐L., McAleer, M.A., Irvine, A.D., Wilson, N.J., Tavadia, S., Schwartz, M.E., Cole, C., Sandilands, A., Smith, F.J.D., Zamiri, M.
Publicado 2017

Mutations in POGLUT1 in Galli–Galli/Dowling–Degos disease

por Wilson, N.J., Cole, C., Kroboth, K., Hunter, W.N., Mann, J.A., McLean, W.H.I., Kernland Lang, K., Beltraminelli, H., Sabroe, R.A., Tiffin, N., Sobey, G.J., Borradori, L., Simpson, E., Smith, F.J.D.
Publicado 2016

Characteristics of a Widespread Community Cluster of H275Y Oseltamivir-Resistant A(H1N1)pdm09 Influenza in Australia

por Hurt, A. C., Hardie, K., Wilson, N. J., Deng, Y. M., Osbourn, M., Leang, S. K., Lee, R. T. C., Iannello, P., Gehrig, N., Shaw, R., Wark, P., Caldwell, N., Givney, R. C., Xue, L., Maurer-Stroh, S., Dwyer, D. E., Wang, B., Smith, D. W., Levy, A., Booy, R., Dixit, R., Merritt, T., Kelso, A., Dalton, C., Durrheim, D., Barr, I. G.
Publicado 2012