Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

BMC genomic data - 16 Mar 2026

Chen Liping, Zhang Xuemei, Song Yi, Chen Li, He Yongjun, Li Yang, Cai Yan, Shi Qi

Abstract excerpt

OBJECTIVE: To determine CGG repeat numbers in the Fragile X messenger ribonucleoprotein 1 (FMR1) gene among 1,146 women of childbearing age in Northeast Sichuan, China, and to describe regional carrier prevalence. METHODS: A total of 1146 cases of women of childbearing age, voluntarily participating in FMR1 gene detection, were enrolled in this study from April 2021 to January 2024 in our outpatient clinic for...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to China
Share to Cross-Sectional Studies
Share to Fragile X Syndrome

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Pregnancy

Share to Trinucleotide Repeat Expansion

Share to Trinucleotide Repeats

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 41840477
DOI: 10.1186/s12863-026-01417-7
PMCID: PMC13104335

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 17 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of CGG repeat numbers in the FMR1 gene among women of childbearing age in Northeast Sichuan.PMID 41840477Read ↗

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

Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy.Semantic proximity Read ↗

Identification of fragile X pre-mutation carriers in the Chinese obstetric population using a robust FMR1 polymerase chain reaction assay: implications for screening and prenatal diagnosis.Semantic proximity Read ↗

FMR1 allele frequencies in 51,000 newborns: a large-scale population study in China.Semantic proximity Read ↗

FMR1 and the fragile X syndrome: human genome epidemiology review.Semantic proximity Read ↗

Fragile X syndrome carrier screening in pregnant women in Chinese Han population.Semantic proximity Read ↗

Prevalence of CGG expansions of the FMR1 gene in a US population-based sample.Semantic proximity Read ↗

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

An information-rich CGG repeat primed PCR that detects the full range of fragile X expanded alleles and minimizes the need for southern blot analysis.Semantic proximity Read ↗

EMQN best practice guidelines for the molecular genetic testing and reporting of fragile X syndrome and other fragile X-associated disorders.Semantic proximity Read ↗

Refining reproductive risk for FMR1 premutation carriers in the general obstetric population.Semantic proximity Read ↗

ACMG Standards and Guidelines for fragile X testing: a revision to the disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics and Genomics.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.