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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.Human Genetics|January 1, 1984
Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequencesH M Kingston, M Sarfarazi, N S Thomas, et al.American Journal of Human Genetics|July 1, 1992
Anticipation in myotonic dystrophy: new light on an old problemP S Harper, H G Harley, W Reardon, et al.Journal of Medical Genetics|February 1, 1983
Huntington's chorea in South Wales: mutation, fertility, and genetic fitnessD A Walker, P S Harper, R G Newcombe, et al.Pageof 23