Hearing loss and history of otolaryngological conditions in adults with microdeletion 22q11.2
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
Published in American journal of medical genetics. Part A (01.03.2024)
Published in American journal of medical genetics. Part A (01.03.2024)
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Journal Article
Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study
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.
Published in American journal of medical genetics. Part A (01.02.2022)
Published in American journal of medical genetics. Part A (01.02.2022)
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Journal Article
Post-traumatic stress in adults with 22q11.2 deletion syndrome
von Scheibler, Emma N. M. M., van Amelsvoort, Thérèse A. M. J., Vingerhoets, Claudia, van Eeghen, Agnies M., Boot, Erik
Published in BJPsych open (07.07.2022)
Published in BJPsych open (07.07.2022)
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Journal Article
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review
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
Published in Movement disorders clinical practice (Hoboken, N.J.) (01.01.2023)
Published in Movement disorders clinical practice (Hoboken, N.J.) (01.01.2023)
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Journal Article