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Chinnery, PF, Thorburn, DR, Samuels, DC, White, SL, Dahl, HM, Turnbull, DM, Lightowlers, RN, Howell, N.
The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?.
Trends Genet
16(11)
:
500 -505
2000
view publication
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Kirby, DM, Kahler, SG, Freckmann, ML, Reddihough, D, Thorburn, DR.
Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families..
Ann Neurol
48(1)
:
102 -104
2000
view publication
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Dahl, HH, Thorburn, DR, White, SL.
Towards reliable prenatal diagnosis of mtDNA point mutations: studies of nt8993 mutations in oocytes, fetal tissues, children and adults..
Hum Reprod
15 Suppl 2:
246 -255
2000
view publication
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Chow, CW, Thorburn, DR.
Morphological correlates of mitochondrial dysfunction in children..
Hum Reprod
15 Suppl 2:
68 -78
2000
view publication
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Thorburn, DR.
Practical problems in detecting abnormal mitochondrial function and genomes..
Hum Reprod
15 Suppl 2:
57 -67
2000
view publication