Cita APA

Higuchi, S., Takagi, M., Shimomura, S., Nishimura, G., & Hasegawa, Y. (2016). A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1. Clin Pediatr Endocrinol.

Citación estilo Chicago

Higuchi, Shinji, Masaki Takagi, Satoshi Shimomura, Gen Nishimura, y Yukihiro Hasegawa. "A Japanese Familial Case of Schmid Metaphyseal Chondrodysplasia With a Novel mutation in COL10A1." Clin Pediatr Endocrinol 2016.

Cita MLA

Higuchi, Shinji, et al. "A Japanese Familial Case of Schmid Metaphyseal Chondrodysplasia With a Novel mutation in COL10A1." Clin Pediatr Endocrinol 2016.