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Reduction in the number of CGG repeats on the FMR1 gene in carriers of genetic disorders versus noncarriers
OBJECTIVE: CGG repeat expansion on the fragile X mental retardation 1 (FMR1) gene is used to diagnose fragile X syndrome. Previous studies have discussed the correlation between the number of CGG repeats and its associated phenotypic components. The objective of this study is to determine whether th...
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| Publicado no: | JBRA Assist Reprod |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Brazilian Society of Assisted Reproduction
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5714600/ https://ncbi.nlm.nih.gov/pubmed/28967713 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5935/1518-0557.20170054 |
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