Standardization of PCR amplification for fragile X trinucleotide repeat measurements*
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2002.610103.x/fullpdf
Reference20 articles.
1. Interruption of the fragile X syndrome expanded sequence d (CGG) (n) by interspersed d (AGG) trinucleotides diminishes the formation and stability of d (CGG) (n) tetrahelical structures;Weisman-Shomer;Nucl Acid Res,2000
2. Prevalence of carriers of premutation-size alleles of the FMRI gene - and implications for the population genetics of the fragile X syndrome;Rousseau;Am J Hum Genet,1995
3. Tissue-specific methylation differences in a fragile X premutation carrier;Tassone;Clin Genet,1999
4. 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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