Prevalence of Lysosomal Storage Disorders
Meikle, Peter J, Hopwood, John J, Clague, Alan E, Carey, William F
Published in JAMA : the journal of the American Medical Association (20.01.1999)
Published in JAMA : the journal of the American Medical Association (20.01.1999)
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Journal Article
Looking Back on Feb. 2, 2011
Published in Sun-journal (Lewiston, Me.)
(02.02.2011)
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Newspaper Article
Type 2 Gaucher disease: the collodion baby phenotype revisited
Stone, D L, Carey, W F, Christodoulou, J, Sillence, D, Nelson, P, Callahan, M, Tayebi, N, Sidransky, E
Published in Archives of disease in childhood. Fetal and neonatal edition (01.03.2000)
Published in Archives of disease in childhood. Fetal and neonatal edition (01.03.2000)
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Journal Article
Formic acid is a product of the α-oxidation of fatty acids by human skin fibroblasts : deficiency of formic acid production in peroxisome-deficient fibroblasts
POULOS, A, SHARP, P, SINGH, H, JOHNSON, D. W, CAREY, W. F, EASTON, C
Published in Biochemical journal (01.06.1993)
Published in Biochemical journal (01.06.1993)
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Journal Article
FIRST-TRIMESTER DIAGNOSIS OF SMITH-LEMLI-OPITZ SYNDROME
SHARP, P., HAAN, E., FLETCHER, J. M., KHONG, T. Y., CAREY, W. F.
Published in Prenatal diagnosis (01.04.1997)
Published in Prenatal diagnosis (01.04.1997)
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Journal Article
Frequency of intron 8 CFTR polythymidine sequence variant in neonatal blood specimens
Chin, S, Ranieri, E, Gerace, RL, Nelson, PV, Carey, WF
Published in The Lancet (British edition) (08.11.1997)
Published in The Lancet (British edition) (08.11.1997)
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Journal Article
Prenatal diagnosis of mucolipidosis II-electron microscopy and biochemical evaluation
Carey, W. F., Jaunzems, A., Richardson, M., Fong, B. A., Chin, S. J., Nelson, P. V.
Published in Prenatal diagnosis (01.03.1999)
Published in Prenatal diagnosis (01.03.1999)
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Journal Article
Metachromatic leukodystrophy: a nonsense mutation (Q486X) in the arylsulphatase A (ARSA) gene
Harvey, J S, Carey, W F, Nelson, P V, Morris, C P
Published in Human molecular genetics (01.01.1994)
Published in Human molecular genetics (01.01.1994)
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Journal Article
A case of combined Farber and Sandhoff disease
Fusch, C, Huenges, R, Moser, H W, Sewell, A C, Roggendorf, W, Kustermann-Kuhn, B, Poulos, A, Carey, W F, Harzer, K
Published in European journal of pediatrics (01.04.1989)
Published in European journal of pediatrics (01.04.1989)
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Journal Article
Pitfalls in the prenatal diagnosis of peroxisomal beta-oxidation defects by chorionic villus sampling
Carey, W F, Poulos, A, Sharp, P, Nelson, P V, Robertson, E F, Hughes, J L, Gill, A
Published in Prenatal diagnosis (01.09.1994)
Published in Prenatal diagnosis (01.09.1994)
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Journal Article
Prenatal diagnosis of Zellweger's syndrome by chorionic villus sampling--and a caveat
Carey, W F, Robertson, E F, van Crugten, C, Poulos, A, Nelson, P V, Finikiotis, G
Published in Prenatal diagnosis (01.05.1986)
Published in Prenatal diagnosis (01.05.1986)
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Journal Article
Cystic fibrosis: prenatal diagnosis and carrier detection by DNA analysis
Nelson, P V, Carey, W F, Morris, C P, Pollard, A C
Published in Medical journal of Australia (07.08.1989)
Published in Medical journal of Australia (07.08.1989)
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Journal Article
The frequency of the common (delta F508) cystic fibrosis mutation in the Australian population
Nelson, P V, Carey, W F, Morris, C P, Pollard, A C
Published in Medical journal of Australia (19.03.1990)
Published in Medical journal of Australia (19.03.1990)
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