D. M. Broadhead

Clinical findings in 12 patients with MPS IV A (Morquio's disease)

John W. Nelson, D. M. Broadhead, Jean Mossman · Clinical Genetics · 1988 · 66 citations

Full expression of Hunter's disease in a female with an X‐chromosome deletion leading to non‐random inactivation

D. M. Broadhead, J M Kirk, Andrew Burt et al. · Clinical Genetics · 1986 · 49 citations

Heparan Sulphates, Mendelian Disorder, Allergy +13

Low arylsulphatase A activity in a family without metachromatic leukodystrophy

J. Butterworthi, D. M. Broadhead, A. J. Keay · Clinical Genetics · 1978 · 44 citations

Foamy changes of placental cells in probable beta glucuronidase deficiency associated with hydrops fetalis.

J Nelson, Bryan Kenny, Denise M. O’Hara et al. · Journal of Clinical Pathology · 1993 · 39 citations · Full text

Mps Vii, Fetal Medicine, Pathology +22

Recognition of abnormal lysosomal enzyme patterns in childhood leukaemia by isoelectric focusing, with special reference to some properties of abnormally expressed components

D. M. Broadhead, G. T. N. Besley, Stephen Moss et al. · Leukemia Research · 1981 · 33 citations

Chromatin, Biochemistry, Cytogenetics +12