Specific Mutations in Methyl-CpG-Binding Protein 2 Confer Different Severity in Rett Syndrome

Por Neul, J. L., Fang, P., Barrish, J., Lane, J., Caeg, E., Smith, E. O., Zoghbi, H., Percy, A., Glaze, D. G.
Publicado em 2008

Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype‐phenotype correlations

Por Sahoo, T, Peters, S U, Madduri, N S, Glaze, D G, German, J R, Bird, L M, Barbieri‐Welge, R, Bichell, T J, Beaudet, A L, Bacino, C A
Publicado em 2006

Epilepsy and the natural history of Rett syndrome

Por Glaze, D. G., Percy, A. K., Skinner, S., Motil, K. J., Neul, J. L., Barrish, J. O., Lane, J. B., Geerts, S. P., Annese, F., Graham, J., McNair, L., Lee, H. -S.
Publicado em 2010

Clinical severity and quality of life in children and adolescents with Rett syndrome

Por Lane, J.B., Lee, H.-S., Smith, L.W., Cheng, P., Percy, A.K., Glaze, D.G., Neul, J.L., Motil, K.J., Barrish, J.O., Skinner, S.A., Annese, F., McNair, L., Graham, J., Khwaja, O., Barnes, K., Krischer, J.P.
Publicado em 2011