Optometry in adults with microdeletion 22q11.2: The eye as a window to the brain von von Scheibler, Emma N.M.M., Appaji, Abhishek, Berendschot, Tos T.J.M., Bauer, Noël J.C., Rao, Naren P., van Eeghen, Agnies M., van Amelsvoort, Thérèse A.M.J., Boot, Erik

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Hearing loss and history of otolaryngological conditions in adults with microdeletion 22q11.2 von Scheibler, Emma N. M. M., Widdershoven, Josine C. C., Barneveld, Denise C. P. B. M., Schröder, Nina, Eeghen, Agnies M., Amelsvoort, Thérèse A. M. J., Boot, Erik

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Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review von Scheibler, Emma N.M.M., Eeghen, Agnies M., Koning, Tom J., Kuijf, Mark L., Zinkstok, Janneke R., Müller, Annelieke R., Amelsvoort, Thérèse A.M.J., Boot, Erik

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Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study von Scheibler, Emma N. M. M., Valk Bouman, Emy S., Nuijts, Myrthe A., Bauer, Noël J. C., Berendschot, Tos T. J. M., Vermeltfoort, Pit, Bok, Levinus A., Eeghen, Agnies M., Houben, Michiel L., Amelsvoort, Thérèse A. M. J., Boot, Erik, Egmond‐Ebbeling, Michelle B.

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Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review von von Scheibler, Emma N.M.M, van Eeghen, Agnies M, de Koning, Tom J, Kuijf, Mark L, Zinkstok, Janneke R, Müller, Annelieke R, van Amelsvoort, Thérèse A.M.J, Boot, Erik

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