Page 151 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma
P. 151
Chapter 5
Ocular findings in 22q11.2
deletion syndrome:
A systematic literature
review and results of a Dutch
multicenter study
Emma von Scheibler, Emy van der Valk Bouman, Myrthe Nuijts, Noël Bauer,
Tos Berendschot, Pit Vermeltvoort, Levinus Bok, Agnies van Eeghen, Michiel
Houben, Thérèse van Amelsvoort, Erik Boot, Michelle van Egmond-Ebbeling
American Journal of Medical Genetics part A, 2021, 188(2):569-578
