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P S Harper

Showing results (141-150 of 345) with videos related to

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Journal of the Royal College of Physicians of London|July 1, 1996
Clinical genetics services into the 21st century. Summary of a report of the Clinical Genetics Committee of the Royal College of PhysiciansP S Harper, H B Hughes, J A Raeburn
Lancet (London, England)|September 15, 1984
False positive creatine kinase test in hypothyroid male at risk for Duchenne muscular dystrophyH Williams, I Hughes, P S Harper, et al.
Human Mutation|January 1, 1997
Six novel mutations in the neurofibromatosis type 1 (NF1) geneM Upadhyaya, J Maynard, M Osborn, et al.
Journal of Medical Genetics|December 1, 1989
Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment biasP W Lunt, D A Compston, P S Harper
Lancet (London, England)|April 13, 1985
Prenatal diagnosis of Duchenne dystrophyP S Harper, H Williams, N Thomas, et al.
Journal of Medical Genetics|January 5, 2002
Presymptomatic testing in myotonic dystrophy: genetic counselling approachesS Fokstuen, J Myring, C Evans, et al.
Lancet (London, England)|August 9, 1986
First-trimester prediction in fetus at risk for myotonic dystrophyP W Lunt, A L Meredith, P S Harper
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 8, 1982
In vitro studies on calcium activated phosphatidylinositol phosphodiesterase of erythrocyte ghosts from normal individuals and those with myotonic muscular dystrophyA L Meredith, P S Harper, D M Bradley
Brain : a Journal of Neurology|December 1, 1988
Von Recklinghausen neurofibromatosis. A clinical and population study in south-east WalesS M Huson, P S Harper, D A Compston
Lancet (London, England)|July 25, 1992
Detection of minimum mutation carriers in myotonic dystrophyP S Harper, H H Harley, D J Shaw
Pageof 35

Showing results (141-150 of 345) with videos related to

Sort By:
Pageof 35
Journal of the Royal College of Physicians of London|July 1, 1996
Clinical genetics services into the 21st century. Summary of a report of the Clinical Genetics Committee of the Royal College of PhysiciansP S Harper, H B Hughes, J A Raeburn
Lancet (London, England)|September 15, 1984
False positive creatine kinase test in hypothyroid male at risk for Duchenne muscular dystrophyH Williams, I Hughes, P S Harper, et al.
Human Mutation|January 1, 1997
Six novel mutations in the neurofibromatosis type 1 (NF1) geneM Upadhyaya, J Maynard, M Osborn, et al.
Journal of Medical Genetics|December 1, 1989
Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment biasP W Lunt, D A Compston, P S Harper
Lancet (London, England)|April 13, 1985
Prenatal diagnosis of Duchenne dystrophyP S Harper, H Williams, N Thomas, et al.
Journal of Medical Genetics|January 5, 2002
Presymptomatic testing in myotonic dystrophy: genetic counselling approachesS Fokstuen, J Myring, C Evans, et al.
Lancet (London, England)|August 9, 1986
First-trimester prediction in fetus at risk for myotonic dystrophyP W Lunt, A L Meredith, P S Harper
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 8, 1982
In vitro studies on calcium activated phosphatidylinositol phosphodiesterase of erythrocyte ghosts from normal individuals and those with myotonic muscular dystrophyA L Meredith, P S Harper, D M Bradley
Brain : a Journal of Neurology|December 1, 1988
Von Recklinghausen neurofibromatosis. A clinical and population study in south-east WalesS M Huson, P S Harper, D A Compston
Lancet (London, England)|July 25, 1992
Detection of minimum mutation carriers in myotonic dystrophyP S Harper, H H Harley, D J Shaw
Pageof 35