Associated Papers
Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in FMR1 and Associated Phenotypes.
Tekendo-Ngongang C et al.
Genes, 2021
Rare FMR1 gene mutations causing fragile X syndrome: A review.
Sitzmann AF et al.
American Journal of Medical Genetics. Part A, 2018
Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males.
Collins SC et al.
American Journal of Medical Genetics. Part A, 2010
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