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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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Detalhes bibliográficos
Publicado no:JBRA Assist Reprod
Main Authors: Peyser, Alexandra, Singer, Tomer, Mullin, Christine, Hershlag, Avner
Formato: Artigo
Idioma:Inglês
Publicado em: Brazilian Society of Assisted Reproduction 2017
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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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