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Article

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

JBRA assisted reproduction - 1 Dec 2017

Peyser Alexandra, Singer Tomer, Mullin Christine, Hershlag Avner

Abstract excerpt

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 the number of CGG repeats differ between carriers of genetic disorders versus noncarriers. METHODS: We performed a...

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Source

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Identifiers

PMID: 28967713
DOI: 10.5935/1518-0557.20170054
PMCID: PMC5714600

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.

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