Nagata, T., Matsushita, M., Mishima, K., Kamiya, Y., Kato, K., Toyama, M., . . . Kitoh, H. (2020). Severe achondroplasia due to two de novo variants in the transmembrane domain of FGFR3 on the same allele: A case report. Mol Genet Genomic Med.
Citação norma ChicagoNagata, Tadashi, Masaki Matsushita, Kenichi Mishima, Yasunari Kamiya, Kohji Kato, Miho Toyama, Tomoo Ogi, Naoki Ishiguro, and Hiroshi Kitoh. "Severe Achondroplasia Due to Two De Novo Variants in the Transmembrane Domain of FGFR3 On the Same Allele: A Case Report." Mol Genet Genomic Med 2020.
MLA citiranjeNagata, Tadashi, et al. "Severe Achondroplasia Due to Two De Novo Variants in the Transmembrane Domain of FGFR3 On the Same Allele: A Case Report." Mol Genet Genomic Med 2020.