Jing Chen, Qinqin Xiang, Xiao Xiao, Bocheng Xu, Hanbing Xie, He Wang, . . . Shanling Liu. (2022). Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: An affected family. BMC.
Chicago Style (17th ed.) CitationJing Chen, Qinqin Xiang, Xiao Xiao, Bocheng Xu, Hanbing Xie, He Wang, Mei Yang, and Shanling Liu. Carrying Both COL1A2 and FBN2 Gene Heterozygous Mutations Results in a Severe Skeletal Clinical Phenotype: An Affected Family. BMC, 2022.
MLA (9th ed.) CitationJing Chen, et al. Carrying Both COL1A2 and FBN2 Gene Heterozygous Mutations Results in a Severe Skeletal Clinical Phenotype: An Affected Family. BMC, 2022.
Warning: These citations may not always be 100% accurate.