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Delatycki, MB, Paris, DBBP, Gardner, RJM, Nicholson, GA, Nassif, N, Storey, E, MacMillan, JC, Collins, V, Williamson, R, Forrest, SM.
Clinical and genetic study of Friedreich ataxia in an Australian population.
American Journal of Medical Genetics
87(2)
:
168 -174
1999
view publication
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AMOR, D, DELATYCKI, MB, SUSMAN, M, CASEY, E, NASH, T, WARNE, G, HUTSON, J.
46,XX/46,XY at amniocentesis in a fetus with true hermaphroditism.
Journal of Medical Genetics
36(11)
:
866
1999
view publication
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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.
Human Genetics
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.
Annals of Neurology
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.
Journal of Medical Genetics
36(4)
:
335
1999
view publication