Complementation analysis in patients with the clinical phenotype of a generalised peroxisomal disorder.

Por Steinberg, S J, Fensom, A H
Publicado em 1996

The chemical composition of the lipopolysaccharide of Pseudomonas aeruginosa

Por Fensom, A. H., Gray, G. W.
Publicado em 1969

Prenatal Diagnosis of Galactosaemia

Por Fensom, A. H., Benson, P. F., Blunt, S.
Publicado em 1974

Corneal clouding in GM1-generalized gangliosidosis.

Por Babarik, A., Benson, P. F., Fensom, A. H.
Publicado em 1976

Complementation studies in Niemann-Pick disease type C indicate the existence of a second group.

Por Steinberg, S J, Ward, C P, Fensom, A H
Publicado em 1994

Letter: Schilder's disease: cholesterol metabolism in cultured fibroblasts.

Por Benson, P F, Fensom, A H, Wilson, J
Publicado em 1976

Sialic acid storage disease.

Por Cameron, P D, Dubowitz, V, Besley, G T, Fensom, A H
Publicado em 1990

Amniotic cell 4-methylumbelliferyl-alpha-glucosidase activity for prenatal diagnosis of Pompe's disease.

Por Fensom, A H, Benson, P F, Blunt, S, Brown, S P, Coltart, T M
Publicado em 1976

Tay-Sachs disease heterozygote detection: use of a centrifugal analyser for automation of hexosaminidase assays with two different artificial substrates.

Por Landels, E C, Ellis, I H, Bobrow, M, Fensom, A H
Publicado em 1991

X-linked adrenoleukodystrophy with non-diagnostic plasma very long chain fatty acids.

Por Kennedy, C R, Allen, J T, Fensom, A H, Steinberg, S J, Wilson, R
Publicado em 1994

Prenatal diagnosis of argininosuccinic aciduria: effect of mycoplasma contamination on the indirect assay for argininosuccinate lyase.

Por Fensom, A H, Benson, P F, Baker, J E, Mutton, D E
Publicado em 1980

Gaucher's disease in the United Kingdom: screening non-Jewish patients for the two common mutations.

Por Walley, A J, Barth, M L, Ellis, I, Fensom, A H, Harris, A
Publicado em 1993

Prenatal diagnosis of a galactosaemia heterozygote by fetal blood enzyme assay.

Por Fensom, A H, Benson, P F, Rodeck, C H, Campbell, S, Gould, J D
Publicado em 1979

Beta-hexosaminidase splice site mutation has a high frequency among non-Jewish Tay-Sachs disease carriers from the British Isles.

Por Landels, E C, Green, P M, Ellis, I H, Fensom, A H, Bobrow, M
Publicado em 1992

Frequency of the Tay-Sachs disease splice and insertion mutations in the UK Ashkenazi Jewish population.

Por Landels, E C, Ellis, I H, Fensom, A H, Green, P M, Bobrow, M
Publicado em 1991

Characterization of three alleles causing aspartylglycosaminuria: two from a British family and one from an American patient.

Por Park, H, Vettese, M B, Fensom, A H, Fisher, K J, Aronson, N N
Publicado em 1993

Argininosuccinate lyase: a new autoantigen in liver disease

Por PELLI, N, FENSOM, A H, SLADE, C, BOA, F, MIELI-VERGANI, G, VERGANI, D
Publicado em 1998

Further investigation of the HEXA gene intron 9 donor splice site mutation frequently found in non-Jewish Tay-Sachs disease patients from the British Isles.

Por Landels, E C, Green, P M, Ellis, I H, Fensom, A H, Kaback, M M, Lim-Steele, J, Zeiger, K, Levy, N, Bobrow, M
Publicado em 1993

Sixteen years' experience of counselling, diagnosis, and prenatal detection in one genetic centre: progress, results, and problems.

Por Polani, P E, Alberman, E, Alexander, B J, Benson, P F, Berry, A C, Blunt, S, Daker, M G, Fensom, A H, Garrett, D M, McGuire, V M, Roberts, J A, Seller, M J, Singer, J D
Publicado em 1979