Items where authors include "Pippucci, T."

Article

Roychaudhury, A. orcid.org/0000-0003-1497-4909, Lee, Y., Choi, T. et al. (36 more authors) (2024) SRPK3 Is essential for cognitive and ocular development in humans and zebrafish, explaining X-linked intellectual disability. Annals of Neurology, 96 (5). pp. 914-931. ISSN 0364-5134

McNeill, A., Iovino, E., Mansard, L. et al. (17 more authors) (2020) SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect. Brain, 143 (8). pp. 2380-2387. ISSN 0006-8950

Zawerton, A., Yao, B., Yeager, J.P. et al. (13 more authors) (2019) De Novo SOX4 variants cause a neurodevelopmental disease associated with mild dysmorphism. The American Journal of Human Genetics, 104 (2). pp. 246-259. ISSN 0002-9297