Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq.

Author:

Xiang F,Zhang Z,Clarke A,Joseluiz P,Sakkubai N,Sarojini B,Delozier-Blanchet C D,Hansmann I,Edstrom L,Anvret M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference17 articles.

1. Ramos 0. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases;Hagberg, B.; Aicardi, J.; Dias, K.;Ann Neurol,1983

2. Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome X;Journel, H.; Melki, J.; Turleau, C.; Munnich, A.; de Grouchy, J.;Amn J Med Genet,1990

3. A de novo X; 3 translocation in Rett syndrome;Zoghbi, H.Y.; Ledbetter, D.H.; Schultz, R.; Percy, A.K.; Glaze, D.G.;Anm J Med Genet,1990

4. Congenital Rett syndrome phenotype-deletion short arm chromosome 3. Paper presented at the World Congress on Rett syndrome, Gothenburg;Wahlstrom, J.; Uller, A.; Tonnby, B.; Darnfors, C.; Martinsson, T.; Vujic, M.,1996

5. Congenital Rett syndrome phenotype-interstitial deletion chromosome 13 and retinoblastoma. Paper presented at the World Congress on Rett syndrome, Gothenburg,1996

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