Details
Role
Clinical Geneticist
Group
Clinical Services
Top Publications
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Wang, Y, Gurrin, LC, Wluka, AE, Bertalli, NA, Osborne, NJ, Delatycki, MB, Giles, GG, English, DR, Hopper, JL, Simpson, JA, et al.
HFE C282Y Homozygosity Is Associated with an Increased Risk of Total Hip Replacement for Osteoarthritis.
Seminars in Arthritis and Rheumatism
41(6)
:
872 -878
2012
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Delatycki, MB, Wolthuizen, M, Collins, V, Varley, E, Craven, J, Allen, KJ, Gurrin, LC, Aitken, M, Trembath, MK, Bond, L, et al.
ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible.
European Journal of Human Genetics
20(5)
:
505 -509
2012
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Szmulewicz, D, MacDougall, H, Curthoys, I, O'Leary, S, Paine, M, Cremer, P, Delatycki, M, Corben, L, Halmagyi, M.
Impairment of the Vestibulo-Cerebellar Interaction in Friedreich's Ataxia (P02.252).
Neurology
78(Meeting Abstracts 1)
:
p02.252 -p02.252
2012
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Evans‐Galea, MV, Carrodus, N, Rowley, SM, Corben, LA, Tai, G, Saffery, R, Galati, JC, Wong, NC, Craig, JM, Lynch, DR, et al.
FXN methylation predicts expression and clinical outcome in Friedreich ataxia.
Annals of Neurology
71(4)
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487 -497
2012
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Delatycki, MB.
The ethics of screening for disease.
Pathology
44(2)
:
63 -68
2012
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