Wang, X., Zhang, G., Lu, Y., Luo, X., & Wu, W. (2020). Trio‐WES reveals a novel de novo missense mutation of KMT2A in a Chinese patient with Wiedemann‐Steiner syndrome: A case report. Mol Genet Genomic Med.
Citação norma ChicagoWang, Xiong, Guijiao Zhang, Yanjun Lu, Xiaoping Luo, and Wei Wu. "Trio‐WES Reveals a Novel De Novo Missense Mutation of KMT2A in a Chinese Patient With Wiedemann‐Steiner Syndrome: A Case Report." Mol Genet Genomic Med 2020.
Citação norma MLAWang, Xiong, et al. "Trio‐WES Reveals a Novel De Novo Missense Mutation of KMT2A in a Chinese Patient With Wiedemann‐Steiner Syndrome: A Case Report." Mol Genet Genomic Med 2020.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.