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Expanded alleles of the FMR1 gene are related to unexplained recurrent miscarriages
Up to 50% of recurrent miscarriage cases in women occur without an underlying etiology. In the current prospective case–control study, we determined the impact of CGG trinucleotide expansions of the fragile-X mental retardation 1 (FMR1) gene in 49 women with unexplained recurrent miscarriages. Case...
Autores principales: | Wang, Xin-hua, Song, Xiao-hua, Wang, Yan-lin, Diao, Xing-hua, Li, Tong, Li, Qing-chun, Zhang, Xiang-hui, Deng, Xiao-hui |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700269/ https://www.ncbi.nlm.nih.gov/pubmed/29054962 http://dx.doi.org/10.1042/BSR20170856 |
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