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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...
Sparad:
| Huvudupphovsmän: | , , , , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
1991
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| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC328620/ https://ncbi.nlm.nih.gov/pubmed/1886762 |
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