Search Results - "MECP2"

Perspectives on hand function in girls and women with Rett syndrome by Downs, Jennepher, Parkinson, Stephanie, Ranelli, Sonia, Leonard, H., Diener, P., Lotan, M.

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Early development and regression in Rett Syndrome by Lee, J.Y.L., Leonard, H., Piek, Jan Patricia, Downs, Jennepher

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Longitudinal hand function in Rett syndrome by Downs, Jennepher, Bebbington, A., Kaufmann, W., Leonard, H.

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p.R270X MECP2 mutation and mortality in Rett syndrome by Jian, Le, Archer, H., Ravine, D., Kerr, A., De Klerk, N., Christodoulou, J., Bailey, M.

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Atypical Presentations and Specific Genotypes Are Associated With a Delay in Diagnosis in Females With Rett Syndrome by Fehr, S., Downs, Jennepher, Bebbington, A., Leonard, H.

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Seizures in rett syndrom: An overview from a one-year calendar study by Jian, Le, Nagarajan, L., De Klerk, N., Ravine, D., Christodoulou, J., Leonard, H.

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The imprinted gene and parent-of-origin effect database now includes parental origin of de novo mutations. by Glaser, R.L., Ramsay, Josh, Morison, I.M.

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Using directed-content analysis to identify a framework for understanding quality of life in adults with Rett syndrome by Strugnell, A., Leonard, H., Epstein, A., Downs, Jennepher

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