Quantitative measurement of FMRP in blood platelets as a new screening test for fragile X syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2011.01798.x/fullpdf
Reference20 articles.
1. Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.;Coffee;Am J Hum Genet,2009
2. Prevalence of fragile X syndrome.;Turner;Am J Med Genet,1996
3. Absence of expression of the FMR-1 gene in fragile X syndrome.;Pieretti;Cell,1991
4. Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: a case report and review of the literature.;Coffee;Am J Med Genet,2008
5. Fragile X: a family of disorders.;Chonchaiya;Adv Pediatr,2009
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