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Normal intellectual skills in patients with Rhombencephalosynapsis.
Bonnetain MF, Rougeot-Jung C, Sarret C, Lion-François L, Revol O, Peyric E, Velazquez-Dominguez J, Miret A, Rossi M, Massoud M, Laurichesse-Delmas H, Guibaud L, des Portes V. Bonnetain MF, et al. Among authors: miret a. Eur J Paediatr Neurol. 2020 Nov;29:92-100. doi: 10.1016/j.ejpn.2020.09.007. Epub 2020 Sep 30. Eur J Paediatr Neurol. 2020. PMID: 33046393
Neuropsychological study in 19 French patients with White-Sutton syndrome and POGZ mutations.
Garde A, Cornaton J, Sorlin A, Moutton S, Nicolas C, Juif C, Geneviève D, Perrin L, Khau-Van-Kien P, Smol T, Vincent-Delorme C, Isidor B, Cogné B, Afenjar A, Keren B, Coubes C, Prieur F, Toutain A, Trousselet Y, Bourgouin S, Gonin-Olympiade C, Giraudat K, Piton A, Gérard B, Odent S, Tessier F, Lemasson L, Heide S, Gelineau AC, Sarret C, Miret A, Schaefer E, Piard J, Mathevet R, Boucon M, Bruel AL, Mau-Them FT, Chevarin M, Vitobello A, Philippe C, Thauvin-Robinet C, Faivre L. Garde A, et al. Among authors: miret a. Clin Genet. 2021 Mar;99(3):407-417. doi: 10.1111/cge.13894. Epub 2020 Dec 15. Clin Genet. 2021. PMID: 33277917
Discovering the ANK2-related autism phenotype.
Guissart C, Polge A, Durand N, Miret A, Lumbroso S, Francannet C, Mouzat K. Guissart C, et al. Among authors: miret a. Clin Genet. 2023 Sep;104(3):384-386. doi: 10.1111/cge.14347. Epub 2023 Apr 23. Clin Genet. 2023. PMID: 37088467