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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Hlavní autoři: Nakahori, Y, Knight, S J, Holland, J, Schwartz, C, Roche, A, Tarleton, J, Wong, S, Flint, T J, Froster-Iskenius, U, Bentley, D
Médium: Artigo
Jazyk:Inglês
Vydáno: 1991
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC328620/
https://ncbi.nlm.nih.gov/pubmed/1886762
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