Browsing by Author Bailey, Mark E

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Issue DateTitleAuthor(s)Citation
2007Association analysis of the ACTN3 R577X polymorphism and complex quantitative body composition and performance phenotypes in adolescent GreeksMacArthur, Daniel; North, Kathryn; Yang, Nan; Bailey, Mark E; Jamurtas, Athanasios; Moran, Colin N; Pitsiladis, Yannis; Tsiokanos, Athanasios; Wilson, Richard; Medicine; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research InsAssociation analysis of the ACTN3 R577X polymorphism and complex quantitative body composition and performance phenotypes in adolescent Greeks, European Journal of Human Genetics (2005), vol.15,(N/A),2007,pp 88-93
2007Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation.Christodoulou, John; Williamson, Sarah; Archer, Hayley; Bailey, Mark E; Charman, Tony; Clarke, Angus; Colvin, Lyn; de Klerk, Nicholas H.; Evans, Julie; Leonard, Helen; Ravine, David; Sampson, Julian; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthCorrelation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation., Journal of Medical Genetics 2005, vol.44,(2),2007,pp 148-152