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Article

Expanded alleles of the FMR1 gene are related to unexplained recurrent miscarriages.

Bioscience reports - 22 Dec 2017

Wang Xin-Hua, Song Xiao-Hua, Wang Yan-Lin, Diao Xing-Hua, Li Tong, Li Qing-Chun, Zhang Xiang-Hui, Deng Xiao-Hui

Abstract excerpt

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 group consisted of women with two or more unexplained consecutive miscarriages. Blood samples were obtained and...

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Source

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Identifiers

PMID: 29054962
DOI: 10.1042/BSR20170856
PMCID: PMC5700269

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Research trail→

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Expanded alleles of the FMR1 gene are related to unexplained recurrent miscarriages.PMID 29054962Read ↗

[Significance and case analysis of FMR1 mutation screening during early and middle pregnancy].Semantic proximity Read ↗

Reduction in the number of CGG repeats on the FMR1 gene in carriers of genetic disorders versus noncarriers.Semantic proximity Read ↗

Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand?Semantic proximity Read ↗

PGT-M for Premature Ovarian Failure Related to CGG Repeat Expansion of the FMR1 Gene.Semantic proximity Read ↗

Diminished ovarian reserve is not observed in infertility patients with high normal CGG repeats on the fragile X mental retardation 1 (FMR1) geneSemantic proximity Read ↗

Maternal FMR1 alleles expansion in newborns during transmission: a prospective cohort study.Semantic proximity Read ↗

Non-CGG trinucleotide repeat expansions as pathogenic genetic mutations in Fragile X SyndromeSemantic proximity Read ↗

Analysis of CGG repeat numbers in the FMR1 gene among women of childbearing age in Northeast Sichuan.Semantic proximity Read ↗

Both cis and trans-acting genetic factors drive somatic instability in female carriers of the FMR1 premutation.Semantic proximity Read ↗

CGG repeat expansion at FMR1 locus - A new molecular diagnostic algorithm in fragile X syndrome.Semantic proximity Read ↗

A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome.Semantic proximity Read ↗

[Results of carrier screening and prenatal diagnosis for FMR1 gene in 819 cases].Semantic proximity Read ↗

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