Biblio
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Filters: Author is Hagerman,Randi J [Clear All Filters]
[3233] FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States.
Genome Medicine. 4(12),
(2012). [2102] Epigenetic Modification of the FMR1 Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056.
Science Translational Medicine. 3(64), 64ra1 - 64ra1.
(2011). [886] A solution to limitations of cognitive testing in children with intellectual disabilities: the case of fragile X syndrome.
Journal of Neurodevelopmental Disorders. 1(1), 33 - 45.
(2009).