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Clinical 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 HarperDevelopmental Medicine and Child Neurology|February 1, 1984
Course, prognosis and complications of childhood-onset myotonic dystrophyT A O'Brien, P S HarperJournal of Medical Genetics|April 1, 1992
Age at onset and life table risks in genetic counselling for Huntington's diseaseP S Harper, R G NewcombePageof 30