Browsing by Author Ho, G

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Issue DateTitleAuthor(s)Citation
2008Costeff optic atrophy syndrome: New clinical case and novel molecular findingsChristodoulou, John; Ho, G; Walter, John; Children's Hospital Westmead: Paediatrics & Child HealthCosteff optic atrophy syndrome: New clinical case and novel molecular findings, Journal of Inherited Metabolic Disease (JIMD), vol.134,(N/A),2008,pp Online-N/A
2007Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiencyCarpenter, Kevin; Chiong, Mary; Christodoulou, John; Ho, G; Olsen, R. K. J.; Rhead, W; Sim, K. G.; Children's Hospital Westmead: Medicine; Children's Hospital Westmead: Medicine; Children's Hospital Westmead: Paediatrics & Child HealthTransient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency, Molecular Genetics and Metabolism (2005), vol.92,(39479),2007,pp 109-114
2010Updating the profile of C-terminal MECP2 deletions in Rett syndromeChristodoulou, John; Anderson, Alison; Bahi-Buisson, Nadia; Bebbington, Ami; Ben Zeev, B; Ho, G; Jacoby, Peter; Leonard, Helen; Percy, Alan K.; Pineda, M; Ravine, David; Smeets, E; Children's Hospital Westmead: Paediatrics & Child HealthUpdating the profile of C-terminal MECP2 deletions in Rett syndrome, Journal of Medical Genetics, vol.47, N/A,pp 242-248