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Cardiovascular Research|January 1, 1997
Cardiac disease in myotonic dystrophyM F Phillips, P S HarperJournal of Medical Genetics|August 3, 2000
Ten years of presymptomatic testing for Huntington's disease: the experience of the UK Huntington's Disease Prediction ConsortiumP S Harper, C Lim, D CraufurdClinical Genetics|September 1, 1976
Genetic risks in Perthes' diseaseP S Harper, B J Brotherton, D CochlinClinical Genetics|June 1, 1983
Blood pressure and myotonic dystrophyT O'Brien, P S Harper, R G NewcombeClinical Genetics|January 23, 1999
Predictive testing for Huntington's disease: I. Predictors of uptake in South WalesJ Binedell, J R Soldan, P S HarperHuman Mutation|January 1, 1994
Molecular basis of neurofibromatosis type 1 (NF1): mutation analysis and polymorphisms in the NF1 geneM Upadhyaya, D J Shaw, P S HarperBMJ (Clinical Research Ed.)|October 1, 1988
Molecular genetics in clinical practice: evolution of a DNA diagnostic serviceA L Meredith, M Upadhyaya, P S HarperJournal of Medical Genetics|January 1, 1996
Molecular genetics of neurofibromatosis type 1 (NF1)M H Shen, P S Harper, M UpadhyayaJournal of Neurology, Neurosurgery, and Psychiatry|April 1, 1995
Molecular diagnostic analysis for Huntington's disease: a prospective evaluationJ C MacMillan, P Davies, P S HarperJournal of Medical Genetics|January 1, 1992
Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales familiesJ C MacMillan, M Upadhyaya, P S HarperPageof 30