Molecular Correlates and Recent Advancements in the Diagnosis and Screening of FMR1-Related Disorders
Author:
Publisher
MDPI AG
Subject
Genetics(clinical),Genetics
Link
http://www.mdpi.com/2073-4425/7/10/87/pdf
Reference172 articles.
1. FMR1-Related Disorders;Saul,1993
2. Repeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disorders
3. The FMRP regulon: from targets to disease convergence
4. MosaicFMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: A case report and review of the literature
5. A point mutation in the FMR-1 gene associated with fragile X mental retardation
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