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Correlation between clinical severity in Rett syndrome patients with a p.R168X or p.T158M MECP2 mutation and the direction and degree of skewing of X chromosome inactivation

By H Archer, J Evans, H Leonard, L Colvin, D Ravine, J Christodoulou, S Williamson, Tony Charman, M. E. S. Bailey, J Sampson, N de Clerk, A Clarke and M.E.S Bailey
Year: 2007
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