Validation of clinical exome sequencing in the diagnostic procedure of patients with intellectual disability in clinical practice.

MLA

Ballesta-Martínez, María Juliana, et al. “Validation of Clinical Exome Sequencing in the Diagnostic Procedure of Patients with Intellectual Disability in Clinical Practice.” Orphanet Journal of Rare Diseases, vol. 18, no. 1, July 2023, pp. 1–10. EBSCOhost, https://doi.org/10.1186/s13023-023-02809-z.

APA

Ballesta-Martínez, M. J., Pérez-Fernández, V., López-González, V., Sánchez-Soler, M. J., Serrano-Antón, A. T., Rodríguez-Peña, L. I., Barreda-Sánchez, M., Armengol-Dulcet, L., & Guillén-Navarro, E. (2023). Validation of clinical exome sequencing in the diagnostic procedure of patients with intellectual disability in clinical practice. Orphanet Journal of Rare Diseases, 18(1), 1–10. https://doi.org/10.1186/s13023-023-02809-z

Chicago

Ballesta-Martínez, María Juliana, Virginia Pérez-Fernández, Vanesa López-González, María José Sánchez-Soler, Ana Teresa Serrano-Antón, Lidia Isolina Rodríguez-Peña, Maria Barreda-Sánchez, Lluís Armengol-Dulcet, and Encarna Guillén-Navarro. 2023. “Validation of Clinical Exome Sequencing in the Diagnostic Procedure of Patients with Intellectual Disability in Clinical Practice.” Orphanet Journal of Rare Diseases 18 (1): 1–10. doi:10.1186/s13023-023-02809-z.