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Seminars in Thrombosis and Hemostasis|April 1, 2006
Membrane cofactor protein and factor I: mutations and transplantationDavid Kavanagh, Timothy H J GoodshipHematology. American Society of Hematology. Education Program|December 14, 2011
Atypical hemolytic uremic syndrome, genetic basis, and clinical manifestationsDavid Kavanagh, Timothy H J GoodshipJournal of Medical Genetics|June 1, 1979
May spina bifida result from an X-linked defect in a selective abortion mechanism?J Burn, D GibbensAmerican Journal of Medical Genetics|January 1, 1984
Brief clinical report: neural tube defects as an X-linked conditionM Baraitser, J BurnActa Geneticae Medicae Et Gemellologiae|January 1, 1984
Congenital heart defects and twinningJ Burn, G CorneyClinical Genetics|August 1, 1988
Genetic counselling in hypomelanosis of Ito: case report and reviewC Moss, J BurnJournal of Medical Genetics|May 1, 1991
Sweat testing to identify female carriers of X linked hypohidrotic ectodermal dysplasiaA Clarke, J BurnJournal of Medical Genetics|April 1, 1986
Partial lipoatrophy with insulin resistant diabetes and hyperlipidaemia (Dunnigan syndrome)J Burn, M BaraitserJournal of Molecular Biology|February 20, 2002
Molecular modelling of the C-terminal domains of factor H of human complement: a correlation between haemolytic uraemic syndrome and a predicted heparin binding siteStephen J Perkins, Timothy H J GoodshipPageof 58