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Advanced technologies for the molecular diagnosis of fragile X syndrome
Fragile X syndrome (FXS), a trinucleotide repeat disorder, is the most common heritable form of cognitive impairment. Since the discovery of the FMR1 gene in 1991, great strides have been made in the field of molecular diagnosis for FXS. Cytogenetic analysis, which was the method of diagnosis in the...
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| I publikationen: | Expert Rev Mol Diagn |
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| Huvudupphovsman: | |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2015
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4955806/ https://ncbi.nlm.nih.gov/pubmed/26489042 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1586/14737159.2015.1101348 |
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