Showing results (31-40 of 223) with videos related to
Sort By:
Pageof 23
Developmental 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 NewcombeJournal 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 NewcombeJournal of Medical Genetics|June 1, 1977
Genetic markers in Welsh gypsiesP S Harper, E M Williams, E SunderlandClinical 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 UpadhyayaPageof 23