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Article

Screening for fragile X syndrome in males from specialized institutions in the northeast region of Brazil.

Genetics and molecular research : GMR - 18 Jun 2015

Viveiros M T M, Santos M D C, Dos Santos J M, Viveiros D M, Cavalcante M R M, Caldas A J M, Pimentel M M G

Abstract excerpt

The objective of this study was to perform a study of fragile X syndrome (FXS) in São Luís, Maranhão, in males residing in five specialized institutions. Two hundred thirty-eight males with intel-lectual disability of unknown etiology participated in this study. Blood samples were processed and stored until DNA extraction. Screening for FMR1 gene mutations was performed using non-isotopic polymerase chain...

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Source

Identifiers

PMID: 26125897
DOI: 10.4238/2015.June.18.32

Genes

FMR1

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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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