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

Rett syndrome (RS) is a disease of neurological development. First reported 30 years ago in 1966, its biological and genetic basis remains obscure. RS is commonly thought of as an X linked dominant disorder lethal to hemizygous males. The few familial cases would arise through mosaicism or because o...

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Detalhes bibliográficos
Main Authors: Xiang, F, Zhang, Z, Clarke, A, Joseluiz, P, Sakkubai, N, Sarojini, B, Delozier-Blanchet, C D, Hansmann, I, Edström, L, Anvret, M
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051277/
https://ncbi.nlm.nih.gov/pubmed/9598723
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