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
34828275 (PubMed )
Supplement: genes-12-01669-s001.zip › Supplementary_Table_S5.pdf
Rare FMR1 gene mutations causing fragile X syndrome: A review.
Sitzmann AF et al.
American Journal of Medical Genetics. Part A, 2018
Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screening.
Handt M et al.
Molecular and Cellular Probes, 0
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