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...

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Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2017
Materias:
Research Articles
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

Internet

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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