Martin B. Delatycki
Bruce Lefroy Centre for Genetic Health Research
Murdoch Childrens Research Institute
Parkville
Australia
Name/email consistency: high
- Clinical features of Friedreich ataxia. Delatycki, M.B., Corben, L.A. J. Child Neurol. (2012)
- Implementation of ironXS: a study of the acceptability and feasibility of genetic screening for hereditary hemochromatosis in high schools. Delatycki, M.B., Wolthuizen, M., Collins, V., Varley, E., Craven, J., Allen, K.J., Aitken, M.A., Bond, L., Lockhart, P.J., Wilson, G.R., Macciocca, I., Metcalfe, S.A. Clin. Genet. (2010)
- Listen carefully: LIS1 and DCX MLPA in lissencephaly and subcortical band heterotopia. Delatycki, M.B., Leventer, R.J. Eur. J. Hum. Genet. (2009)
- Evaluating the progression of Friedreich ataxia and its treatment. Delatycki, M.B. J. Neurol. (2009)
- Surgery for equinovarus deformity in Friedreich's ataxia improves mobility and independence. Delatycki, M.B., Holian, A., Corben, L., Rawicki, H.B., Blackburn, C., Hoare, B., Toy, M., Churchyard, A. Clin. Orthop. Relat. Res. (2005)
- A de novo, apparently balanced reciprocal translocation in a child with developmental delay whose mother was being treated with low-dose methotrexate at the time of conception. Delatycki, M.B. Birth Defects Res. Part A Clin. Mol. Teratol. (2005)
- A homozygous HAMP mutation in a multiply consanguineous family with pseudo-dominant juvenile hemochromatosis. Delatycki, M.B., Allen, K.J., Gow, P., MacFarlane, J., Radomski, C., Thompson, J., Hayden, M.R., Goldberg, Y.P., Samuels, M.E. Clin. Genet. (2004)
- Hereditary hemochromatosis genetic testing of at-risk children: what is the appropriate age?. Delatycki, M.B., Powell, L.W., Allen, K.J. Genet. Test. (2004)