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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: 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
Lenguaje:Inglês
Publicado: 1991
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC328620/
https://ncbi.nlm.nih.gov/pubmed/1886762
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares