Suzanne de Bruijn

334 Chapter 8 Smits JJ*, de Bruijn SE *, Lanting CP, Oostrik J, O'Gorman L, Mantere T, DOOFNL Consortium, Cremers FPM, Roosing S, Yntema HG, de Vrieze E, Derks R, Hoischen A, Pegge SAH, Neveling K, Pennings RJE, Kremer H. Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant. Human Genetics , in press. de Vrieze*, de Bruijn SE *, Reurink J, Broekman S, van de Riet V, Aben M, Kremer H, van Wijk E. Efficient generation of knock-in zebrafish models for inherited disorders using CRISPR-Cas9 ribonucleoprotein complexes. International Journal of Molecular Sciences 22 , 9429-9445 (2021).