Article Versions Notes

González-del Angel A, Alcántara-Ortigoza MA, Ramos S, Algara-Ramírez C, Hernández-Hernández MA, Saenger-Rivas L. Unusual Trisomy X Phenotype Associated with a Concurrent Heterozygous 16p11.2 Deletion: Importance of an Integral Approach for Proper Diagnosis. International Journal of Molecular Sciences. 2023; 24(19):14643. https://doi.org/10.3390/ijms241914643

González-del Angel, Ariadna, Miguel Angel Alcántara-Ortigoza, Sandra Ramos, Carolina Algara-Ramírez, Marco Antonio Hernández-Hernández, and Lorenza Saenger-Rivas. 2023. "Unusual Trisomy X Phenotype Associated with a Concurrent Heterozygous 16p11.2 Deletion: Importance of an Integral Approach for Proper Diagnosis" International Journal of Molecular Sciences 24, no. 19: 14643. https://doi.org/10.3390/ijms241914643

González-del Angel, A., Alcántara-Ortigoza, M. A., Ramos, S., Algara-Ramírez, C., Hernández-Hernández, M. A., & Saenger-Rivas, L. (2023). Unusual Trisomy X Phenotype Associated with a Concurrent Heterozygous 16p11.2 Deletion: Importance of an Integral Approach for Proper Diagnosis. International Journal of Molecular Sciences, 24(19), 14643. https://doi.org/10.3390/ijms241914643