Page 253 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma
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About the author
E.N.M.M. von Scheibler, M. Kuijf, T.J. de Koning, J.R. Zinkstok, A. Muller,
T.A.M.J. van Amelsvoort, A.M. van Eeghen, H.J.G. Boot. Parkinsonism in
individuals with rare genetic neurodevelopmental disorders: A systematic
review. Poster presentation at the Society of the Study of Behavioral
Phenotypes conference, 2021.
Emma N.M.M. von Scheibler, Josine C.C. Widdershoven, Denise C.P.B.M.
van Barneveld, Nina Schröder, Agnies M. van Eeghen, Thérèse A.M.J. van
Amelsvoort, Erik Boot. Age-related high-frequency hearing loss in adults
with microdeletion 22q11.2. Oral presentation; 6th IASSIDD Europe congress
2021, Amsterdam, the Netherlands.
Emma N.M.M. von Scheibler, Emy S. van der Valk Bouman, Tos T.J.M.
Berendschot, Noël J.C. Bauer, Levinus A. Bok, Pit B.J. Vermeltfoort , Thérèse
A.M.J. van Amelsvoort, Agnies M. van Eeghen, Michiel Houben, Erik Boot,
Michelle B. van Egmond. Ocular findings in 142 individuals with 22q11.2
deletion syndrome. Oral presentation; 6th IASSIDD Europe congress 2021,
Amsterdam, Netherlands.
Grants
Les and Robbie Fountain bursary award by the Society of the Study of
Behavioral Phenotypes (SSBP) to attend the international SSBP conference
in Oslo, 2022.
Mobility grant by the European Graduate School of Neuroscience for a
one-month research and clinical internship at the Department of Human
Genetics, University Hospital Leuven, Belgium.
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