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Paulet, Alix; Bennett-Ness, Cavan; Ageorges, Faustine; Trost, Detlef; Green, Andrew; Goudie, David; Jewell, Rosalyn; Kraatari-Tiri, Minna; Piard, Juliette; Coubes, Christine; Lam, Wayne; Lynch, Sally Ann; Groeschel, Samuel; Ramond, Francis; Fluss, Joël; Fagerberg, Christina; Brasch Andersen, Charlotte; Varvagiannis, Konstantinos; Kleefstra, Tjitske; Gérard, Bénédicte; ... (2024). Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study. European journal of human genetics, 32(9), p. 1191. Springer Nature 10.1038/s41431-024-01606-x
Ruaud, Lyse; Drunat, Séverine; Elmaleh-Bergès, Monique; Ernault, Anais; Guilmin Crepon, Sophie; The MCPH, Consortium; El Ghouzzi, Vincent; Auvin, Stéphane; Verloes, Alain; Passemard, Sandrine (2022). Neurological outcome in WDR62 primary microcephaly. Developmental medicine and child neurology, 64(4), pp. 509-517. Wiley 10.1111/dmcn.15060
