C. E. Hatton

Accelerated telomere shortening in young recipients of allogeneic bone-marrow transplants

Robert Wynn, Michael Cross, C. E. Hatton et al. · The Lancet · 1998 · 233 citations

Life Sciences, Genetics, Immunology +13

Mutation analysis in 46 British and Irish patients with Gaucher's disease

C. E. Hatton, Alan Cooper, C. Whitehouse et al. · Archives of Disease in Childhood · 1997 · 81 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Mutation analysis in 57 unrelated patients with MPS II (Hunter's disease)

Elizabeth Vafiadaki, Alan Cooper, Lesley Heptinstall et al. · Archives of Disease in Childhood · 1998 · 80 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Human β‐mannosidase deficiency: Biochemical findings in plasma, fibroblasts, white cells and urine

Alan Cooper, C. E. Hatton, Margaret J. Thornley et al. · Journal of Inherited Metabolic Disease · 1987 · 53 citations

Life Sciences, Biochemistry, Molecular Biology +3

Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrow.

LJ Fairbairn, L. S. Lashford, Elaine Spooncer et al. · Proceedings of the National Academy of Sciences · 1996 · 50 citations · Full text

Life Sciences, Biotechnology, Molecular Biology +14