Vaz, S. O., Pires, R., Pires, L. M., Carreira, I. M., Anjos, R., Maciel, P., & Mota-Vieira, L. (2015). A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: A report of two cases. BMC Pediatr.
Citação norma ChicagoVaz, Sara O., Renato Pires, Luís M. Pires, Isabel M. Carreira, Rui Anjos, Paula Maciel, and Luisa Mota-Vieira. "A Unique Phenotype in a Patient With a Rare Triplication of the 22q11.2 Region and New Clinical Insights of the 22q11.2 Microduplication Syndrome: A Report of Two Cases." BMC Pediatr 2015.
MLA引文Vaz, Sara O., et al. "A Unique Phenotype in a Patient With a Rare Triplication of the 22q11.2 Region and New Clinical Insights of the 22q11.2 Microduplication Syndrome: A Report of Two Cases." BMC Pediatr 2015.