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Clinical Genetics|July 11, 2017
Phenotypic spectrum associated with de novo mutations in QRICH1 geneA Ververi, M Splitt, J C S Dean, et al.Journal of Medical Genetics|July 1, 1990
Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasiaJ Goodship, S Malcolm, A Clarke, et al.Current Opinion in Nephrology and Hypertension|July 10, 2002
The genetics and pathogenesis of haemolytic uraemic syndrome and thrombotic thrombocytopenic purpuraAnna Richards, Judith A Goodship, Timothy H J GoodshipJournal of Medical Genetics|March 1, 1988
Intellectual development in Apert's syndrome: a long term follow up of 29 patientsM A Patton, J Goodship, R Hayward, et al.Pediatric Nephrology (Berlin, Germany)|May 17, 2008
Plasma therapy in atypical haemolytic uremic syndrome: lessons from a family with a factor H mutationJean Claude Davin, Lisa Strain, Tim H J GoodshipAmerican Journal of Medical Genetics. Part A|May 12, 2006
A constitutional telomeric translocation showing meiotic instabilityD J Josifova, R Mazzaschi, T Ballard, et al.Journal of Medical Genetics|October 1, 1993
DiGeorge syndrome: part of CATCH 22D I Wilson, J Burn, P Scambler, et al.Molecular Immunology|July 2, 2013
Complement therapy in atypical haemolytic uraemic syndrome (aHUS)Edwin K S Wong, Tim H J Goodship, David KavanaghJournal of Medical Genetics|January 1, 1988
Service experience using DNA analysis for genetic prediction in Duchenne muscular dystrophyJ Goodship, S Malcolm, M E Robertson, et al.Clinical Dysmorphology|July 1, 1992
New dysmorphic syndrome with choanal atresia in siblingsJ Burn, C McKeown, J Wagget, et al.Pageof 391