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Birth Defects Original Article Series|June 1, 1971
Genetic heterogeneity in hyperkeratosis palmaris et plantarisP S HarperNeuromuscular Disorders : NMD|November 26, 1998
PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafnessM F Phillips, M T Rogers, R Barnetson, et al.Current Opinion in Neurology and Neurosurgery|October 1, 1992
Advances in myotonic dystrophy: a clinical and genetic perspectiveW Reardon, P S HarperJournal of Medical Genetics|June 1, 1983
Attitudes of subjects at risk and their relatives towards genetic counselling in Huntington's choreaA Tyler, P S HarperBritish Medical Journal (Clinical Research Ed.)|June 29, 1985
Genetic prediction and family structure in Huntington's choreaP S Harper, M SarfaraziAnnals of Neurology|September 1, 1991
Single-gene neurological disorders in South Wales: an epidemiological studyJ C MacMillan, P S HarperFASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1992
Presymptomatic testing for late-onset genetic disorders: lessons from Huntington's diseaseD M Ball, P S HarperBritish Medical Bulletin|July 1, 1989
Myotonic dystrophy: developments in molecular geneticsD J Shaw, P S HarperArchives of Disease in Childhood|November 1, 1982
Mild form of Hunter's syndrome: clinical delineation based on 31 casesI D Young, P S HarperPageof 23