Items where authors include "Pippucci, T."
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Number of items: 2.
Article
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