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P S Harper

Showing results (161-170 of 345) with videos related to

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Journal of Biosocial Science|April 1, 1983
Family break-down and stress in Huntington's choreaA Tyler, P S Harper, K Davies, et al.
Journal of Medical Genetics|September 1, 1989
Duchenne muscular dystrophy in Wales: a 15 year study, 1971 to 1986A M Norman, C Rogers, J R Sibert, et al.
Archives of Disease in Childhood|March 1, 1986
The use of flanking markers in prediction for Duchenne muscular dystrophyH Williams, M Sarfarazi, C Brown, et al.
American Journal of Human Genetics|June 1, 1991
Genetic risks for children of women with myotonic dystrophyM C Koch, T Grimm, H G Harley, et al.
Journal of Medical Genetics|June 1, 1980
Ichthyosis, hepatosplenomegaly, and cerebellar degeneration in a sibshipP S Harper, R Marks, P J Dykes, et al.
Journal of Genetic Counseling|July 5, 2015
Psychological Model for Presymptomatic Test Interviews: Lessons Learned from Huntington DiseaseJ Soldan, E Street, J Gray, et al.
Journal of Medical Genetics|June 1, 1988
Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocationJ Zonana, S H Roberts, N S Thomas, et al.
The British Journal of Psychiatry : the Journal of Mental Science|February 1, 1997
Huntington's disease: psychiatric practice in molecular genetic prediction and diagnosisJ Scourfield, J Soldan, J Gray, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2003
Familial motor neurone disease with dementia: phenotypic variation and cerebellar pathologyT M Polvikoski, A Murray, P S Harper, et al.
Journal of Medical Genetics|November 1, 1989
A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severityS M Huson, D A Compston, P Clark, et al.
Pageof 35

Showing results (161-170 of 345) with videos related to

Sort By:
Pageof 35
Journal of Biosocial Science|April 1, 1983
Family break-down and stress in Huntington's choreaA Tyler, P S Harper, K Davies, et al.
Journal of Medical Genetics|September 1, 1989
Duchenne muscular dystrophy in Wales: a 15 year study, 1971 to 1986A M Norman, C Rogers, J R Sibert, et al.
Archives of Disease in Childhood|March 1, 1986
The use of flanking markers in prediction for Duchenne muscular dystrophyH Williams, M Sarfarazi, C Brown, et al.
American Journal of Human Genetics|June 1, 1991
Genetic risks for children of women with myotonic dystrophyM C Koch, T Grimm, H G Harley, et al.
Journal of Medical Genetics|June 1, 1980
Ichthyosis, hepatosplenomegaly, and cerebellar degeneration in a sibshipP S Harper, R Marks, P J Dykes, et al.
Journal of Genetic Counseling|July 5, 2015
Psychological Model for Presymptomatic Test Interviews: Lessons Learned from Huntington DiseaseJ Soldan, E Street, J Gray, et al.
Journal of Medical Genetics|June 1, 1988
Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocationJ Zonana, S H Roberts, N S Thomas, et al.
The British Journal of Psychiatry : the Journal of Mental Science|February 1, 1997
Huntington's disease: psychiatric practice in molecular genetic prediction and diagnosisJ Scourfield, J Soldan, J Gray, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2003
Familial motor neurone disease with dementia: phenotypic variation and cerebellar pathologyT M Polvikoski, A Murray, P S Harper, et al.
Journal of Medical Genetics|November 1, 1989
A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severityS M Huson, D A Compston, P Clark, et al.
Pageof 35