Nagahara, K., Harada, Y., Futami, T., Takagi, M., Nishimura, G., & Hasegawa, Y. (2016). A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3. Clin Pediatr Endocrinol.
Style de citation ChicagoNagahara, Keiko, Yuki Harada, Tohru Futami, Masaki Takagi, Gen Nishimura, et Yukihiro Hasegawa. "A Japanese Familial Case of Hypochondroplasia With a Novel Mutation In FGFR3." Clin Pediatr Endocrinol 2016.
Style de citation MLANagahara, Keiko, et al. "A Japanese Familial Case of Hypochondroplasia With a Novel Mutation In FGFR3." Clin Pediatr Endocrinol 2016.
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