Browsing by Author Vasudevan, V

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Issue DateTitleAuthor(s)Citation
2007Delineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male probandBennetts, Bruce; Christodoulou, John; Slater, Katrina; Vasudevan, V; Williamson, Sarah; Bebbinton, Ami; Cloosterman, Desiree; Donald, Jennifer; Hardwick, Simon A; Leonard, Helen; Reuter, Kirsten; Smith, Robert; Williams, Simon R.; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Paediatrics & Child HealthDelineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male proband, European Journal of Human Genetics (2005), vol.15,(12),2007,pp 1218-1229
2006Lost in translation: translational interference from a recurrent mutation in exon 1 of MECP2.Christodoulou, John; Vasudevan, V; Williamson, Sarah; de Lagarde, D.; Leonard, Helen; Macleod, P.; Ravine, David; Saxena, Alka; Thompson, Elizabeth M.; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Paediatrics & Child HealthLost in translation: translational interference from a recurrent mutation in exon 1 of MECP2., Journal of Medical Genetics 2005, vol.43,(6),2006,pp 470-477