APA (7th ed.) Citation

Lanlan Mi, Ruen Yao, Weiwei Guo, Jian Wang, Guoqing Zhang, & Xiuxia Ye. (2024). Concurrent de novo MACF1 mutation and inherited 16p13.11 microduplication in a preterm newborn with hypotonia, joint hyperlaxity and multiple congenital malformations: A case report. BMC.

Chicago Style (17th ed.) Citation

Lanlan Mi, Ruen Yao, Weiwei Guo, Jian Wang, Guoqing Zhang, and Xiuxia Ye. Concurrent De Novo MACF1 Mutation and Inherited 16p13.11 Microduplication in a Preterm Newborn with Hypotonia, Joint Hyperlaxity and Multiple Congenital Malformations: A Case Report. BMC, 2024.

MLA (9th ed.) Citation

Lanlan Mi, et al. Concurrent De Novo MACF1 Mutation and Inherited 16p13.11 Microduplication in a Preterm Newborn with Hypotonia, Joint Hyperlaxity and Multiple Congenital Malformations: A Case Report. BMC, 2024.