Search Results - McKenzie, F.
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Human Genetics Society of Australasia Position Statement: Population-Based Carrier Screening for Cystic Fibrosis by Delatycki, M., Burke, J., Christie, L., Collins, F., Gabbett, M., George, P., Haan, E., Ioannou, L., Martin, N., McKenzie, F., O'Leary, Peter, Scoble-Williams, N., Turner, G., Massie, J.
Published 2014Get full text
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Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance by Woodward, K., Stampalia, J., Vanyai, H., Rijhumal, H., Potts, K., Taylor, F., Peverall, J., Grumball, T., Sivamoorthy, S., Alinejad-Rokny, H., Wray, J., Whitehouse, A., Nagarajan, L., Scurlock, J., Afchani, S., Edwards, M., Murch, A., Beilby, J., Baynam, G., Kiraly-Borri, C., McKenzie, F., Heng, Julian
Published 2019Get full text
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The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical service. by Baynam, G., Pachter, N., McKenzie, F., Townshend, S., Slee, J., Kiraly-Borri, C., Vasudevan, A., Hawkins, A., Broley, S., Schofield, L., Verhoef, H., Walker, C., Molster, C., Blackwell, J., Jamieson, S., Tang, D., Lassmann, T., Mina, K., Beilby, J., Davis, M., Laing, N., Murphy, L., Weeramanthri, T., Dawkins, Hugh, Goldblatt, J.
Published 2016Get full text
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Initiating an undiagnosed diseases program in the Western Australian public health system by Baynam, G., Broley, S., Bauskis, A., Pachter, N., McKenzie, F., Townshend, S., Slee, J., Kiraly-Borri, C., Vasudevan, A., Hawkins, A., Schofield, L., Helmholz, Petra, Palmer, R., Kung, S., Walker, C., Molster, C., Lewis, B., Mina, K., Beilby, J., Pathak, G., Poulton, C., Groza, T., Zankl, A., Roscioli, T., Dinger, M., Mattick, J., Gahl, W., Groft, S., Tifft, C., Taruscio, D., Lasko, P., Kosaki, K., Wilhelm, H., Melegh, B., Carapetis, J., Jana, S., Chaney, G., Johns, A., Owen, P., Daly, F., Weeramanthri, T., Dawkins, H., Goldblatt, J.
Published 2017Get full text