Page 133 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma
P. 133
Chapter 4
Hearing loss and history of
otolaryngologic conditions
in adults with microdeletion
22q11.2
Emma von Scheibler, Josine Widdershoven, Denise van Barneveld,
Nina Schröder, Agnies van Eeghen, Thérèse van Amelsvoort, Erik Boot
Submitted
