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Exploring gastrointestinal health in MECP2 duplication syndrome.
Pehlivan D, Ak M, Glaze DG, Suter B, Motil KJ. Pehlivan D, et al. Among authors: suter b. Neurogastroenterol Motil. 2023 Aug;35(8):e14601. doi: 10.1111/nmo.14601. Epub 2023 Apr 30. Neurogastroenterol Motil. 2023. PMID: 37122114
Current clinical evidence does not support a link between TBL1XR1 and Rett syndrome: Description of one patient with Rett features and a novel mutation in TBL1XR1, and a review of TBL1XR1 phenotypes.
Zaghlula M, Glaze DG, Enns GM, Potocki L, Schwabe AL, Suter B. Zaghlula M, et al. Among authors: suter b. Am J Med Genet A. 2018 Jul;176(7):1683-1687. doi: 10.1002/ajmg.a.38689. Epub 2018 May 19. Am J Med Genet A. 2018. PMID: 29777588 Review. No abstract available.
The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2.
Neul JL, Benke TA, Marsh ED, Skinner SA, Merritt J, Lieberman DN, Standridge S, Feyma T, Heydemann P, Peters S, Ryther R, Jones M, Suter B, Kaufmann WE, Glaze DG, Percy AK. Neul JL, et al. Among authors: suter b. Am J Med Genet B Neuropsychiatr Genet. 2019 Jan;180(1):55-67. doi: 10.1002/ajmg.b.32707. Epub 2018 Dec 7. Am J Med Genet B Neuropsychiatr Genet. 2019. PMID: 30536762 Free PMC article.
Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome.
Peters SU, Fu C, Suter B, Marsh E, Benke TA, Skinner SA, Lieberman DN, Standridge S, Jones M, Beisang A, Feyma T, Heydeman P, Ryther R, Kaufmann WE, Glaze DG, Neul JL, Percy AK. Peters SU, et al. Among authors: suter b. Clin Genet. 2019 May;95(5):575-581. doi: 10.1111/cge.13521. Epub 2019 Mar 15. Clin Genet. 2019. PMID: 30788845 Free PMC article.
Kinematics associated with treadmill walking in Rett syndrome.
Layne CS, Young DR, Lee BC, Glaze DG, Schwabe A, Suter B. Layne CS, et al. Among authors: suter b. Disabil Rehabil. 2021 Jun;43(11):1585-1593. doi: 10.1080/09638288.2019.1674389. Epub 2019 Oct 15. Disabil Rehabil. 2021. PMID: 31613656
204 results