Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Reference137 articles.
1. A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE
2. Incidence of Fragile X Syndrome by Newborn Screening for Methylated FMR1 DNA
3. Origins of the fragile X syndrome mutation.
4. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
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