Cite
MLA Citation
Meina Lin et al.. “Extremely severe scoliosis, heterotopic ossification, and osteoarthritis in a three‐generation family with Crouzon syndrome carrying a mutant c.799T>C FGFR2.” Molecular genetics & genomic medicine, vol. 7, no. 9, 2019, p. n/a. http://access.bl.uk/ark:/81055/vdc_100091284514.0x000009