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Delatycki, MB, Knight, M, Koenig, M, Cossée, M, Williamson, R, Forrest, SM.
G130V, a common FRDA point mutation, appears to have arisen from a common founder..
Hum Genet
105(4)
:
343 -346
1999
view publication
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Delatycki, MB, Camakaris, J, Brooks, H, Evans-Whipp, T, Thorburn, DR, Williamson, R, Forrest, SM.
Direct evidence that mitochondrial iron accumulation occurs in Friedreich ataxia..
Ann Neurol
45(5)
:
673 -675
1999
view publication
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Delatycki, MB, Voullaire, L, Francis, D, Petrovic, V, Robertson, A, Webber, LM, Slater, HR.
Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection..
J Med Genet
36(4)
:
335 -338
1999
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Mas, C, Delatycki, MB, Weintraub, RG.
Persistent truncus arteriosus in monozygotic twins: case report and literature review..
Am J Med Genet
82(2)
:
146 -148
1999
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Delatycki, MB, Paris, D, Gardner, RJ, Forshaw, K, Nicholson, GA, Nassif, N, Williamson, R, Forrest, SM.
Sperm DNA analysis in a Friedreich ataxia premutation carrier suggests both meiotic and mitotic expansion in the FRDA gene..
J Med Genet
35(9)
:
713 -716
1998
view publication