Browsing by Author Leonard, H.

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Issue DateTitleAuthor(s)Citation
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