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Leigh syndrome: Clinical features and biochemical and DNA abnormalities

Annals of neurology, 1996-03, Vol.39 (3), p.343-351

1996

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Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1

The Lancet (British edition), 1994-04, Vol.343 (8901), p.824-827

1994

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Mutations of the Flavin-Containing Monooxygenase Gene (FMO3) cause Trimethylaminuria, a Defect in Detoxication

Human molecular genetics, 1998-05, Vol.7 (5), p.839-845

1998

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Copper deficiency in humans

Annual review of nutrition, 1988-01, Vol.8 (1), p.235-257

DANKS, D. M

1988

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Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease

The Lancet (British edition), 1992-11, Vol.340 (8831), p.1330-1333

1992

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Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards

The Lancet (British edition), 1991-08, Vol.338 (8766), p.552-553

1991

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Trimethylaminuria, fish odour syndrome: a new method of detection and response to treatment with metronidazole

Journal of inherited metabolic disease, 1995-05, Vol.18 (3), p.306-312

1995

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Copper and liver disease

European journal of pediatrics, 1991-01, Vol.150 (3), p.142-148

Danks, D M

1991

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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

Prenatal diagnosis, 1995-05, Vol.15 (5), p.455-465

1995

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Hairs from Patients with Maple Syrup Urine Disease Show a Structural Defect in the Fiber Cuticle

Journal of investigative dermatology, 1996-03, Vol.106 (3), p.461-464

1996

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Genetic heterogeneity in osteogenesis imperfecta

Journal of medical genetics, 1979-04, Vol.16 (2), p.101-116

1979

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Testing for Huntington's disease

Medical journal of Australia, 1994-09, Vol.161 (6), p.350-350

Danks, David M

1994

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The natural history of untreated phenylketonuria over 20 years

Journal of paediatrics and child health, 1991-06, Vol.27 (3), p.189-190

1991

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Carrier testing for cystic fibrosis

Medical journal of Australia, 1993-08, Vol.159 (3), p.148-150

Danks, David M

1993

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X‐linked pyruvate dehydrogenase E1α subunit deficiency in heterozygous females: Variable manifestation of the same mutation

Journal of inherited metabolic disease, 1992-11, Vol.15 (6), p.835-847

1992

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X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia

Journal of medical genetics, 1986-02, Vol.23 (1), p.23-31

1986

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Identification of the mutations in the T-protein gene causing typical and atypical nonketotic hyperglycinemia

Human genetics, 1994-06, Vol.93 (6), p.655-658

1994

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Gene therapy and related novel forms of treatment

Medical journal of Australia, 1993-08, Vol.159 (4), p.276-279

Danks, David M

1993

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Defining the location of the Huntington disease gene

American journal of human genetics, 1993-01, Vol.52 (1), p.214-214

Danks, D M

1993

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Whither genetic services?

Medical journal of Australia, 1993-08, Vol.159 (4), p.221-222

Danks, David M

1993

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Some thoughts on the human genome project

Medical journal of Australia, 1990-05, Vol.152 (9), p.488-489

DANKS, D. M

1990

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Of mice and men, metals and mutations

Journal of medical genetics, 1986-04, Vol.23 (2), p.99-106

Danks, D M

1986

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Treatable complications in undiagnosed cases of autosomal dominant polycystic kidney disease

The Lancet (British edition), 1991-01, Vol.337 (8734), p.127-129

1991

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PAEDIATRICIANS' REPORTS TO GENERAL PRACTITIONERS: SHOULD PARENTS RECEIVE COPIES?

Journal of paediatrics and child health, 1994-04, Vol.30 (2), p.190-190

DANKS, D. M.

1994

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DNA diagnostic tests : expanding role and evolving techniques

Medical journal of Australia, 1991-01, Vol.154 (1), p.3-7

DANKS, D. M

1991

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Leigh syndrome: Clinical features and biochemical and DNA abnormalities

Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1

Mutations of the Flavin-Containing Monooxygenase Gene (FMO3) cause Trimethylaminuria, a Defect in Detoxication

Copper deficiency in humans

Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease

Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards

Trimethylaminuria, fish odour syndrome: a new method of detection and response to treatment with metronidazole

Copper and liver disease

New estimates of down syndrome risks at chorionic villus sampling, amniocentesis, and livebirth in women of advanced maternal age from a uniquely defined population

Hairs from Patients with Maple Syrup Urine Disease Show a Structural Defect in the Fiber Cuticle

Genetic heterogeneity in osteogenesis imperfecta

Testing for Huntington's disease

The natural history of untreated phenylketonuria over 20 years

Carrier testing for cystic fibrosis

X‐linked pyruvate dehydrogenase E1α subunit deficiency in heterozygous females: Variable manifestation of the same mutation

X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia

Identification of the mutations in the T-protein gene causing typical and atypical nonketotic hyperglycinemia

Gene therapy and related novel forms of treatment

Defining the location of the Huntington disease gene

Whither genetic services?

Some thoughts on the human genome project

Of mice and men, metals and mutations

Treatable complications in undiagnosed cases of autosomal dominant polycystic kidney disease

PAEDIATRICIANS' REPORTS TO GENERAL PRACTITIONERS: SHOULD PARENTS RECEIVE COPIES?

DNA diagnostic tests : expanding role and evolving techniques

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