Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia

MLA

Fuu Jen Tsai, et al. “Intragenic Microdeletion of RUNX2 Is a Novel Mechanism for Cleidocranial Dysplasia.” Genomic Medicine, vol. 2, Jan. 2008, pp. 45–49. EBSCOhost, https://doi.org/10.1007/s11568-008-9024-y.

APA

Fuu Jen Tsai, Chih Yang Liu, Jer-Yuarn Wu, Ching-Heng Chou, Feng Mei Sun, Pauline Yen, Ming Ta Michael Lee, Yuan-Tsong Chen, Anne Chun Hui Tsai, Li Chen Huang, & Chyi-Chyang Lin. (2008). Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia. Genomic Medicine, 2, 45–49. https://doi.org/10.1007/s11568-008-9024-y

Chicago

Fuu Jen Tsai, Chih Yang Liu, Jer-Yuarn Wu, Ching-Heng Chou, Feng Mei Sun, Pauline Yen, Ming Ta Michael Lee, et al. 2008. “Intragenic Microdeletion of RUNX2 Is a Novel Mechanism for Cleidocranial Dysplasia.” Genomic Medicine 2 (January): 45–49. doi:10.1007/s11568-008-9024-y.