Short Communication Screening for fragile X syndrome in males from specialized institutions in the northeast region of Brazil-Reference-Cited by-同舟云学术

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

Published:2015 Issue:2 Volume:14 Page:6897-6905
ISSN:1676-5680
Container-title:Genetics and Molecular Research
language:
Short-container-title:Genet. Mol. Res.

Author:

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.

Publisher

Genetics and Molecular Research

Subject

Genetics,Molecular Biology,General Medicine

Link

http://www.funpecrp.com.br/gmr/year2015/vol14-2/pdf/gmr5956.pdf

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical and molecular characteristics of FMR1 microdeletion in patient with fragile X syndrome and review of the literature;Clinica Chimica Acta;2024-01

2. Increased Serum Levels of miR-125b and miR-132 in Fragile X Syndrome;Neurology Genetics;2022-10-26

3. Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in FMR1 and Associated Phenotypes;Genes;2021-10-22

4. Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome;European Journal of Human Genetics;2017-02-08

5. Epidemiology of Fragile X Syndrome;Fragile X Syndrome;2017

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