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Public Health|December 11, 1997
Maternal serum screening for Down's syndrome: a survey of midwives' viewsS Fairgrieve, D Magnay, I White, et al.European Journal of Human Genetics : EJHG|January 1, 1996
Audit of maternal serum screening: strategies to augment counselling in response to women's viewsJ Burn, S Fairgrieve, P Franks, et al.Journal of the Royal College of Physicians of London|January 1, 1992
Carrier testing for cystic fibrosis: knowledge and attitudes within a local communityD Magnay, O Wilson, S el Hait, et al.Molecular and Cellular Probes|October 1, 1996
Mutation detection in exons 1-14 of the adenomatous polyposis coli gene: identification of an alternatively spliced transcriptT Hamzehloei, S P West, P Chapman, et al.Journal of Medical Genetics|January 1, 1991
Association of less common cystic fibrosis mutations with a mild phenotypeA Curtis, R Nelson, M Porteous, et al.Journal of Medical Genetics|December 1, 1994
Genetic heterogeneity in hereditary haemorrhagic telangiectasiaM E Porteous, A Curtis, O Williams, et al.Developmental Medicine and Child Neurology|August 1, 1996
Co-dominant inheritance of hyperekplexia and spastic paraparesisP Baxter, S Connolly, A Curtis, et al.Journal of Medical Genetics|July 1, 1992
A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisationJ Goodship, A Curtis, I Cross, et al.Journal of Inherited Metabolic Disease|January 1, 1994
Relevance of the Human Genome Project to inherited metabolic diseaseJ BurnPageof 150