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Nisselle, A, Delatycki, M, Collins, V, Metcalfe, S, Aitken, M, Du Sart, D, Halliday, J, Macciocca, I, Wakefield, A, Hill, V, et al.
Implementation of HaemScreen, a workplace‐based genetic screening program for hemochromatosis.
Clinical Genetics
65(5)
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358 -367
2004
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Turner, G, Lower, K, White, S, Delatycki, M, Lampe, A, Wright, M, Smith, JC, Kerr, B, Schelley, S, Hoyme, H, et al.
The clinical picture of the Börjeson–Forssman–Lehmann syndrome in males and heterozygous females with PHF6 mutations.
Clinical Genetics
65(3)
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226 -232
2004
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Voncken, M, Ioannou, P, Delatycki, MB.
Friedreich ataxia—update on pathogenesis and possible therapies.
neurogenetics
5(1)
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1 -8
2004
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Delatycki, MB, Sheffield, LJ, Wake, S, Cohen, J.
Screening approach for Fragile X syndrome.
Prenatal Diagnosis
24(1)
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67 -68
2004
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Delatycki, M.
Should third party consent to research be mandated? Should there be a right for third parties to have data about them withdrawn from a research project? Two perspectives.
Monash Bioethics Review
23(1)
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s75 -s86
2004
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