Fragile X syndrome and connective tissue dysregulation
Author:
Affiliation:
1. Departamento de Morfología Universidad del Valle; Cali Colombia
2. UC Davis MIND Institute, University of California; Davis California
3. Facultad de Ciencias Naturales y Matemáticas, Universidad del Rosario; Bogotá Colombia
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13469/fullpdf
Reference68 articles.
1. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk;Cell,1991
2. FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States;Tassone;Genome Med,2012
3. Fragile X: a family of disorders;Chonchaiya;Adv Pediatr,2009
4. Potential therapeutic interventions for fragile X syndrome;Levenga;Trends Mol Med,2010
5. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox;Fu;Cell,1991
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