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Archives of Disease in Childhood|November 1, 1982
Mild form of Hunter's syndrome: clinical delineation based on 31 casesI D Young, P S HarperDevelopmental Medicine and Child Neurology|August 1, 1983
The natural history of the severe form of Hunter's syndrome: a study based on 52 casesI D Young, P S HarperJournal of Medical Genetics|August 1, 1982
An unusual form of familial acrocephalosyndactylyI D Young, P S HarperJournal of Neurology, Neurosurgery, and Psychiatry|May 1, 1980
Hereditary distal spinal muscular atrophy with vocal cord paralysisI D Young, P S HarperChild: Care, Health and Development|July 1, 1981
Psychosocial problems in Hunter's syndromeI D Young, P S HarperJournal of Medical Genetics|June 1, 1980
Ichthyosis, hepatosplenomegaly, and cerebellar degeneration in a sibshipP S Harper, R Marks, P J Dykes, et al.Clinical Genetics|November 1, 1982
Mannosidosis in two brothers: prolonged survival in the severe phenotypeM A Patton, I C Barnes, I D Young, et al.American Journal of Medical Genetics|September 1, 1983
Carrier detection in Hunter syndromeI M Archer, I D Young, D W Rees, et al.American Journal of Human Genetics|March 1, 1992
Huntington disease and the abuse of geneticsP S HarperPageof 34