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Vibert R, Mignot C, Keren B, et al. Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication-deletion: Genotype-phenotype correlation for anomalies of the corpus callosum. Clin Genet. 2021;doi: 10.1111/cge.14096.
Vibert, R., Mignot, C., Keren, B., Chantot-Bastaraud, S., Portnoï, M. F., Nouguès, M. C., Moutard, M. L., Faudet, A., Whalen, S., Haye, D., Garel, C., Chatron, N., Rossi, M., Vincent-Delorme, C., Boute, O., Delobel, B., Andrieux, J., Devillard, F., Coutton, C., Puechberty, J., Pebrel-Richard, C., Colson, C., Gerard, M., Missirian, C., Sigaudy, S., Busa, T., Doco-Fenzy, M., Malan, V., Rio, M., Doray, B., Sanlaville, D., Siffroi, J. P., Héron, D., & Heide, S. (2021). Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication-deletion: Genotype-phenotype correlation for anomalies of the corpus callosum. Clinical genetics, . https://doi.org/10.1111/cge.14096
Vibert, Roseline, et al. "Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication-deletion: Genotype-phenotype correlation for anomalies of the corpus callosum." Clinical genetics vol. (2021). doi: https://doi.org/10.1111/cge.14096
Vibert R, Mignot C, Keren B, Chantot-Bastaraud S, Portnoï MF, Nouguès MC, Moutard ML, Faudet A, Whalen S, Haye D, Garel C, Chatron N, Rossi M, Vincent-Delorme C, Boute O, Delobel B, Andrieux J, Devillard F, Coutton C, Puechberty J, Pebrel-Richard C, Colson C, Gerard M, Missirian C, Sigaudy S, Busa T, Doco-Fenzy M, Malan V, Rio M, Doray B, Sanlaville D, Siffroi JP, Héron D, Heide S. Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication-deletion: Genotype-phenotype correlation for anomalies of the corpus callosum. Clin Genet. 2021 Dec 05; doi: 10.1111/cge.14096. Epub 2021 Dec 05. PMID: 34866188.
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