Characteristics of Queensland physicians and the influence of rural exposure on practice location
Runge, C. E., MacKenzie, A., Loos, C., Waller, M., Gabbett, M., Mills, R., Eley, D.
Published in Internal medicine journal (01.08.2016)
Published in Internal medicine journal (01.08.2016)
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Genotype and clinical care correlations in craniosynostosis: Findings from a cohort of 630 Australian and New Zealand patients
Roscioli, T., Elakis, G., Cox, T.C., Moon, D.J., Venselaar, H., Turner, A.M., Le, T., Hackett, E., Haan, E., Colley, A., Mowat, D., Worgan, L., Kirk, E.P., Sachdev, R., Thompson, E., Gabbett, M., McGaughran, J., Gibson, K., Gattas, M., Freckmann, M-L., Dixon, J., Hoefsloot, L., Field, M., Hackett, A., Kamien, B., Edwards, M., Adès, L.C., Collins, F.A., Wilson, M.J., Savarirayan, R., Tan, T.Y., Amor, D.J., McGIllivray, G., White, S.M., Glass, I.A., David, D.J., Anderson, P.J., Gianoutsos, M., Buckley, M.F.
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.11.2013)
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.11.2013)
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Recessive loss-of-function SCN4A mutations associated with a novel phenotype of congenital myopathy
Zaharieva, I, Thor, M, Oates, E, Karnebeek, C, Kamsteeg, E, Hartley, L, Blom, E, Witting, N, Rasmussen, M, Gabbett, M, Ravenscroft, G, Hanna, M, Ruben, P, Lewis, S, Mannikko, R, Muntoni, F
Published in Neuromuscular disorders : NMD (01.10.2015)
Published in Neuromuscular disorders : NMD (01.10.2015)
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Journal Article
Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism
Hämäläinen, RH, Mowat, D, Gabbett, MT, O'Brien, TA, Kallijärvi, J, Lehesjoki, A-E
Published in Clinical genetics (01.12.2006)
Published in Clinical genetics (01.12.2006)
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Prader-Willi syndrome phenocopy due to duplication of Xq21.1-q21.31, with array CGH of the critical region
Gabbett, MT, Peters, GB, Carmichael, JM, Darmanian, AP, Collins, FA
Published in Clinical genetics (01.04.2008)
Published in Clinical genetics (01.04.2008)
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G.P.300 - Recessive loss-of-function SCN4A mutations associated with a novel phenotype of congenital myopathy
Zaharieva, I., Thor, M., Oates, E., Karnebeek, C., Kamsteeg, E., Hartley, L., Blom, E., Witting, N., Rasmussen, M., Gabbett, M., Ravenscroft, G., Hanna, M., Ruben, P., Lewis, S., Mannikko, R., Muntoni, F.
Published in Neuromuscular disorders : NMD (01.10.2015)
Published in Neuromuscular disorders : NMD (01.10.2015)
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Short Report: Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism
Hämäläinen, R H, Mowat, D, Gabbett, M T, O'Brien, T A, Kallijärvi, J, A-E Lehesjoki
Published in Clinical genetics (01.12.2006)
Published in Clinical genetics (01.12.2006)
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