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P S Harper

Showing results (111-120 of 345) with videos related to

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Clinical Genetics|June 1, 1983
Blood pressure and myotonic dystrophyT O'Brien, P S Harper, R G Newcombe
The Journal of Pediatrics|November 1, 1983
Outlook for a clinically normal child in a sibship with congenital myotonic dystrophyT O'Brien, R G Newcombe, P S Harper
Journal of Medical Genetics|June 1, 1977
Genetic markers in Welsh gypsiesP S Harper, E M Williams, E Sunderland
Clinical Genetics|January 23, 1999
Predictive testing for Huntington's disease: I. Predictors of uptake in South WalesJ Binedell, J R Soldan, P S Harper
Human 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 Harper
BMJ (Clinical Research Ed.)|October 1, 1988
Molecular genetics in clinical practice: evolution of a DNA diagnostic serviceA L Meredith, M Upadhyaya, P S Harper
Journal of Medical Genetics|February 1, 1996
Selection for presymptomatic testing for Huntington's disease: who decides?J Binedell, J R Soldan, P S Harper
Journal of Medical Genetics|January 1, 1996
Molecular genetics of neurofibromatosis type 1 (NF1)M H Shen, P S Harper, M Upadhyaya
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1995
Molecular diagnostic analysis for Huntington's disease: a prospective evaluationJ C MacMillan, P Davies, P S Harper
British Medical Journal (Clinical Research Ed.)|October 15, 1983
Implications of diagnostic delay in Duchenne muscular dystrophyT O'Brien, J R Sibert, P S Harper
Pageof 35

Showing results (111-120 of 345) with videos related to

Sort By:
Pageof 35
Clinical Genetics|June 1, 1983
Blood pressure and myotonic dystrophyT O'Brien, P S Harper, R G Newcombe
The Journal of Pediatrics|November 1, 1983
Outlook for a clinically normal child in a sibship with congenital myotonic dystrophyT O'Brien, R G Newcombe, P S Harper
Journal of Medical Genetics|June 1, 1977
Genetic markers in Welsh gypsiesP S Harper, E M Williams, E Sunderland
Clinical Genetics|January 23, 1999
Predictive testing for Huntington's disease: I. Predictors of uptake in South WalesJ Binedell, J R Soldan, P S Harper
Human 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 Harper
BMJ (Clinical Research Ed.)|October 1, 1988
Molecular genetics in clinical practice: evolution of a DNA diagnostic serviceA L Meredith, M Upadhyaya, P S Harper
Journal of Medical Genetics|February 1, 1996
Selection for presymptomatic testing for Huntington's disease: who decides?J Binedell, J R Soldan, P S Harper
Journal of Medical Genetics|January 1, 1996
Molecular genetics of neurofibromatosis type 1 (NF1)M H Shen, P S Harper, M Upadhyaya
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1995
Molecular diagnostic analysis for Huntington's disease: a prospective evaluationJ C MacMillan, P Davies, P S Harper
British Medical Journal (Clinical Research Ed.)|October 15, 1983
Implications of diagnostic delay in Duchenne muscular dystrophyT O'Brien, J R Sibert, P S Harper
Pageof 35