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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Detalles Bibliográficos
Autores principales: Peyser, Alexandra, Singer, Tomer, Mullin, Christine, Hershlag, Avner
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Brazilian Society of Assisted Reproduction 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714600/
https://www.ncbi.nlm.nih.gov/pubmed/28967713
http://dx.doi.org/10.5935/1518-0557.20170054

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714600/
https://www.ncbi.nlm.nih.gov/pubmed/28967713
http://dx.doi.org/10.5935/1518-0557.20170054

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