Unstable triplets and their mutational mechanism: Size reduction of the CGG repeat vs. germline mosaicism in the fragile X syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference33 articles.
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2. Fragile X founder effect?
3. Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development
4. THE ACCOMMODATION OF NONCOMPLEMENTARY BASES IN HELICAL POLYRIBONUCLEOTIDES AND DEOXYRIBONUCLEIC ACIDS
5. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
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4. Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndrome;European Journal of Medical Genetics;2016-09
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