A fragile gene
Author:
Publisher
Wiley
Subject
General Biochemistry, Genetics and Molecular Biology
Reference70 articles.
1. (1991). In Fragile X Syndrome: Diagnosis, Treatment and Research (ed. and ), pp. 1-68. The John Hopkins University Press, Baltimore and London.
2. Neurodevelopmental effects of the FMR-1 full mutation in humans
3. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
4. Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome
5. Fragile X Genotype Characterized by an Unstable Region of DNA
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