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American Journal of Medical Genetics|January 22, 1996
X-inactivation patterns in monozygotic and dizygotic female twinsJ Goodship, J Carter, J BurnHematology. American Society of Hematology. Education Program|December 14, 2011
Atypical hemolytic uremic syndrome, genetic basis, and clinical manifestationsDavid Kavanagh, Timothy H J GoodshipJournal 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 GoodshipThe Journal of Experimental Medicine|June 6, 2007
Complement factor H and the hemolytic uremic syndromeJohn P Atkinson, Timothy H J GoodshipClinical and Experimental Immunology|January 1, 1991
Evidence that X-linked severe combined immunodeficiency is not a differentiation defect of T lymphocytesJ Goodship, S Malcolm, R J LevinskyJournal of Medical Genetics|September 1, 1995
Monozygotic twins with chromosome 22q11 deletion and discordant phenotypeJ Goodship, I Cross, P Scambler, et al.British Medical Bulletin|September 14, 2006
Atypical haemolytic uraemic syndromeDavid Kavanagh, Timothy H J Goodship, Anna RichardsArchives of Disease in Childhood|January 6, 1999
A population study of chromosome 22q11 deletions in infancyJ Goodship, I Cross, J LiLing, et al.Journal of Medical Genetics|October 1, 1991
A male with type I orofaciodigital syndromeJ Goodship, J Platt, R Smith, et al.Clinical and Experimental Dermatology|July 2, 2015
Multifocal capillary malformations in an older, asymptomatic child with a novel RASA1 mutationS Whitaker, S Leech, A Taylor, et al.Pageof 391