Browsing by Author Clarke, A.

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Issue DateTitleAuthor(s)Citation
2001Guidelines for reporting clinical features in cases with MECP2 mutationsChristodoulou, John; Ellaway, Carolyn; Amstrong, D; Anvret, M; Belichenko,, P; Budden, S; Cass, H; Clarke, A.; d'Esposito,, M; et, al; Kerr, Alison; Nomura, Y; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthGuidelines for reporting clinical features in cases with MECP2 mutations, Brain and Development, vol.23, 4,pp 208-211
2003Mutation analysis in the MECP2 gene and genetic councelling for Rett syndromeChristodoulou, John; Cheadle, J. P.; Clarke, A.; Cranston, T.; Davis, M.; Fleming, N.; Gill, H.; Hanefeld, F.; Kerr, A.; Leonard, H.; Maynard, J.; Ravine, D.; Skjeldal, O.; Tandy, A.; Thompson, E. M.; Whatley, Sharon; Children's Hospital Westmead: Paediatrics & Child HealthMutation analysis in the MECP2 gene and genetic councelling for Rett syndrome, Journal of Medical Genetics, vol.40,(N/A),2003,pp 380-384
2003Patients with the R133C mutation: is their phenotype different from patients with Rett syndrome with other mutations?Christodoulou, John; Clarke, A.; Colvin, Lyn; Davis, Mark; de Klerk, Nicholas H.; Fyfe, Susan; Hackwell, S.; Kondo, I.; Leonard, H.; Matsuishi, T.; Ravine, D.; Schiavello, T.; Williamson, Sarah L; Yamashita, Y.; Children's Hospital Westmead: Paediatrics & Child HealthPatients with the R133C mutation: is their phenotype different from patients with Rett syndrome with other mutations?, Journal of Medical Genetics, vol.40,(e52),2003,pp 1-7