Molecular heterogeneity of the fragile X syndrome.

The fragile X syndrome is an X-linked disorder which has been shown to be associated with the length variation of a DNA fragment containing a CGG trinucleotide repeat element at or close to the fragile site. Phenotypically normal carriers of the disorder generally have a smaller length variation tha...

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Detalhes bibliográficos
Publicado no:Nucleic Acids Res
Main Authors: Nakahori, Y, Knight, S J, Holland, J, Schwartz, C, Roche, A, Tarleton, J, Wong, S, Flint, T J, Froster-Iskenius, U, Bentley, D
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 1991
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC328620/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1886762/
https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/19.16.4355
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