Tang, H., Guo, J., Linpeng, S., & Wu, L. (2019, February). Next generation sequencing identified two novel mutations in NIPBL and a frame shift mutation in CREBBP in three Chinese children. Orphanet Journal of Rare Diseases.
Chicago Style (17th ed.) CitationTang, Hui, Jing Guo, Siyuan Linpeng, and Lingqian Wu. "Next Generation Sequencing Identified Two Novel Mutations in NIPBL and a Frame Shift Mutation in CREBBP in Three Chinese Children." Orphanet Journal of Rare Diseases Feb. 2019.
MLA (9th ed.) CitationTang, Hui, et al. "Next Generation Sequencing Identified Two Novel Mutations in NIPBL and a Frame Shift Mutation in CREBBP in Three Chinese Children." Orphanet Journal of Rare Diseases, Feb. 2019.
Warning: These citations may not always be 100% accurate.
