-
Nisselle, AE, Delatycki, MB, Collins, V, Metcalfe, S, Aitken, MA, du Sart, D, Halliday, J, Macciocca, I, Wakefield, A, Hill, V, et al.
Implementation of HaemScreen, a workplace-based genetic screening program for hemochromatosis..
Clin Genet
65(5)
:
358 -367
2004
view publication
-
Turner, G, Lower, KM, White, SM, Delatycki, M, Lampe, AK, Wright, M, Smith, JC, Kerr, B, Schelley, S, Hoyme, HE, et al.
The clinical picture of the Börjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutations..
Clin Genet
65(3)
:
226 -232
2004
view publication
-
Voncken, M, Ioannou, P, Delatycki, MB.
Friedreich ataxia-update on pathogenesis and possible therapies..
Neurogenetics
5(1)
:
1 -8
2004
view publication
-
Delatycki, MB, Powell, LW, Allen, KJ.
Hereditary hemochromatosis genetic testing of at-risk children: what is the appropriate age?.
Genet Test
8(2)
:
98 -103
2004
view publication
-
Pollard, LM, Sharma, R, Gómez, M, Shah, S, Delatycki, MB, Pianese, L, Monticelli, A, Keats, BJB, Bidichandani, SI.
Replication-mediated instability of the GAA triplet repeat mutation in Friedreich ataxia..
Nucleic Acids Res
32(19)
:
5962 -5971
2004
view publication