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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
Schalk, Audrey; Cousin, Margot A; Dsouza, Nikita R; Challman, Thomas D; Wain, Karen E; Powis, Zoe; Minks, Kelly; Trimouille, Aurélien; Lasseaux, Eulalie; Lacombe, Didier; Angelini, Chloé; Michaud, Vincent; Van-Gils, Julien; Spataro, Nino; Ruiz, Anna; Gabau, Elizabeth; Stolerman, Elliot; Washington, Camerun; Louie, Ray; Lanpher, Brendan C; ... (2021). De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability. Journal of medical genetics, 59(10), pp. 965-975. BMJ Publishing Group 10.1136/jmedgenet-2021-107751
