An intragenic duplication in the AFF2 gene associated with Cornelia de Lange syndrome phenotype.

MLA

Lucia-Campos, Cristina, et al. “An Intragenic Duplication in the AFF2 Gene Associated with Cornelia de Lange Syndrome Phenotype.” Frontiers in Genetics, Nov. 2024, pp. 1–15. EBSCOhost, https://doi.org/10.3389/fgene.2024.1472543.

APA

Lucia-Campos, C., Parenti, I., Latorre-Pellicer, A., Gil-Salvador, M., Bestetti, I., Finelli, P., Larizza, L., Arnedo, M., Ayerza-Casas, A., Del Rincón, J., Trujillano, L., Morte, B., Pérez-Jurado, L. A., Lapunzina, P., Leitão, E., Beygo, J., Lich, C., Kilpert, F., Kaya, S., & Depienne, C. (2024). An intragenic duplication in the AFF2 gene associated with Cornelia de Lange syndrome phenotype. Frontiers in Genetics, 1–15. https://doi.org/10.3389/fgene.2024.1472543

Chicago

Lucia-Campos, Cristina, Ilaria Parenti, Ana Latorre-Pellicer, Marta Gil-Salvador, Ilaria Bestetti, Palma Finelli, Lidia Larizza, et al. 2024. “An Intragenic Duplication in the AFF2 Gene Associated with Cornelia de Lange Syndrome Phenotype.” Frontiers in Genetics, November, 1–15. doi:10.3389/fgene.2024.1472543.