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Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing.
Sci Rep. 2019 Oct 25;9(1):15315. doi: 10.1038/s41598-019-51618-7.
Sci Rep. 2019.
PMID: 31653898
Free PMC article.
Feasibility of wearable technology for 'real-world' gait analysis in children with Prader-Willi and Angelman syndromes.
Kraan CM, Date P, Rattray A, Sangeux M, Bui QM, Baker EK, Morison J, Amor DJ, Godler DE.
Kraan CM, et al.
J Intellect Disabil Res. 2022 Aug;66(8-9):717-725. doi: 10.1111/jir.12955. Epub 2022 Jun 17.
J Intellect Disabil Res. 2022.
PMID: 35713265
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