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Hearing loss and history of otolaryngological conditions in adults with microdeletion 22q11.2.
Am J Med Genet A. 2024 Mar;194(3):e63456. doi: 10.1002/ajmg.a.63456. Epub 2023 Nov 2.
Am J Med Genet A. 2024.
PMID: 37916923
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review.
von Scheibler ENMM, van Eeghen AM, de Koning TJ, Kuijf ML, Zinkstok JR, Müller AR, van Amelsvoort TAMJ, Boot E.
von Scheibler ENMM, et al.
Mov Disord Clin Pract. 2022 Oct 31;10(1):17-31. doi: 10.1002/mdc3.13577. eCollection 2023 Jan.
Mov Disord Clin Pract. 2022.
PMID: 36699000
Free PMC article.
Review.
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Post-traumatic stress in adults with 22q11.2 deletion syndrome.
von Scheibler ENMM, van Amelsvoort TAMJ, Vingerhoets C, van Eeghen AM, Boot E.
von Scheibler ENMM, et al.
BJPsych Open. 2022 Jul 7;8(4):e126. doi: 10.1192/bjo.2022.525.
BJPsych Open. 2022.
PMID: 35795982
Free PMC article.
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Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study.
von Scheibler ENMM, van der Valk Bouman ES, Nuijts MA, Bauer NJC, Berendschot TTJM, Vermeltfoort P, Bok LA, van Eeghen AM, Houben ML, van Amelsvoort TAMJ, Boot E, van Egmond-Ebbeling MB.
von Scheibler ENMM, et al.
Am J Med Genet A. 2022 Feb;188(2):569-578. doi: 10.1002/ajmg.a.62556. Epub 2021 Nov 12.
Am J Med Genet A. 2022.
PMID: 34773366
Free PMC article.
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