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Journal of Inherited Metabolic Disease|January 1, 1984
Infantile type 2 sialidosis in a Pakistani family--a clinical and biochemical studyM King, F Cockburn, G B MacPhee, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|February 28, 1990
A new sensitive microassay for the measurement of erythrocyte glycogenJ Farquharson, E C Jamieson, G B MacPhee, et al.Archives of Disease in Childhood|October 1, 1993
Malonyl coenzyme A decarboxylase deficiencyG B MacPhee, R W Logan, J S Mitchell, et al.Journal of Mental Deficiency Research|June 1, 1982
A slowly progressive degenerative condition characterized by mental deficiency, wasting of limb musculature and bone abnormalities, including ossification of the pinnaeD A PrimroseJournal of Mental Deficiency Research|September 1, 1979
Treatment of self-injurious behaviour with a GABA (gamma-aminobutyric acid) analogueD A PrimroseJournal of Mental Deficiency Research|September 1, 1975
Epiloia in twins: a problem in diagnosis and counsellingD A PrimroseJournal of Mental Deficiency Research|December 1, 1983
Phenylketonuria with normal intelligenceD A PrimroseThe British Journal of Psychiatry : the Journal of Mental Science|January 1, 1984
Changing sociological and clinical patterns in mental handicap. The 1983 Blake Marsh lectureD A PrimroseBritish Journal of Urology|April 1, 1982
Cryptorchism in cerebral palsyJ S Rundle, D A Primrose, R CarachiClinical Dysmorphology|January 1, 1996
A neuropsychiatric disorder associated with dense calcification of the external ears and distal muscle wasting: 'Primrose syndrome'N M Lindor, A D Hoffman, D A PrimrosePageof 6