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AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome
PURPOSE: The ability to accurately predict the likelihood of expansion of the CGG repeats in the FMR1 gene to a full mutation is of critical importance for genetic counseling of women who are carriers of premutation alleles (55–200 CGG repeats) and who are weighing the risk of having a child with fr...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3990283/ https://ncbi.nlm.nih.gov/pubmed/22498846 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2012.34 |
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