Leigh syndrome: clinical features and biochemical and DNA abnormalities
Rahman, S, Blok, R B, Dahl, H H, Danks, D M, Kirby, D M, Chow, C W, Christodoulou, J, Thorburn, D R
Published in Annals of neurology (01.03.1996)
Published in Annals of neurology (01.03.1996)
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Mutations of the Flavin-Containing Monooxygenase Gene (FMO3) cause Trimethylaminuria, a Defect in Detoxication
Treacy, E. P., Akerman, B. R., Chow, L. M. L., Youil, R., Lin, C. Bibeau, J., Bruce, A. G., Knight, M., Danks, D. M., Cashman, J. R., Forrest, S. M.
Published in Human molecular genetics (01.05.1998)
Published in Human molecular genetics (01.05.1998)
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Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards
Matsubara, Y., Narisawa, K., Ye-Qi, Y., Tada, K., Ikeda, H., Danks, D.M., Green, A., McCabe, E.R.B.
Published in The Lancet (British edition) (31.08.1991)
Published in The Lancet (British edition) (31.08.1991)
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Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease
Ravine, D, Forrest, S.M, Sheffield, L.J, Danks, D.M, Walker, R.G, Kincaid-Smith, P, Gibson, R.N, Richards, R.I., Friend, K.
Published in The Lancet (British edition) (28.11.1992)
Published in The Lancet (British edition) (28.11.1992)
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Hairs from Patients with Maple Syrup Urine Disease Show a Structural Defect in the Fiber Cuticle
Jones, L.N., Peet, D.J., Danks, D.M., Negri, A.P., Rivett, D.E.
Published in Journal of investigative dermatology (01.03.1996)
Published in Journal of investigative dermatology (01.03.1996)
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New estimates of Down syndrome risks at chorionic villus sampling, amniocentesis, and livebirth in women of advanced maternal age from a uniquely defined population
Halliday, J L, Watson, L F, Lumley, J, Danks, D M, Sheffield, L J
Published in Prenatal diagnosis (01.05.1995)
Published in Prenatal diagnosis (01.05.1995)
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X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia
Halliday, J, Chow, C W, Wallace, D, Danks, D M
Published in Journal of medical genetics (01.02.1986)
Published in Journal of medical genetics (01.02.1986)
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X-linked pyruvate dehydrogenase E1 alpha subunit deficiency in heterozygous females: variable manifestation of the same mutation
Dahl, H H, Hansen, L L, Brown, R M, Danks, D M, Rogers, J G, Brown, G K
Published in Journal of inherited metabolic disease (01.11.1992)
Published in Journal of inherited metabolic disease (01.11.1992)
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Identification of the mutations in the T-protein gene causing typical and atypical nonketotic hyperglycinemia
Nanao, K, Okamura-Ikeda, K, Motokawa, Y, Danks, D M, Baumgartner, E R, Takada, G, Hayasaka, K
Published in Human genetics (01.06.1994)
Published in Human genetics (01.06.1994)
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