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Developmental 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 HarperClinical Genetics|October 1, 1992
The Charcot-Marie-Tooth syndrome: perceptions of disability and projected use of DNA diagnostic testsJ C MacMillan, P S HarperClinical Genetics|March 1, 1994
The Charcot-Marie-Tooth syndrome: clinical aspects from a population study in South Wales, UKJ C MacMillan, P S HarperClinica Chimica Acta; International Journal of Clinical Chemistry|February 1, 1978
Myotonic dystrophy: studies on the lipid composition and metabolism of erythrocytes and skin fibroblastsN S Thomas, P S HarperAmerican Journal of Medical Genetics|December 1, 1986
A molecular approach to genetic counseling in the X-linked muscular dystrophiesP S Harper, N S ThomasJournal of Medical Genetics|October 1, 1991
Genetic counselling in facioscapulohumeral muscular dystrophyP W Lunt, 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 HarperPageof 23