Cite
HARVARD Citation
Nagata, T. et al. (2020). Severe achondroplasia due to two de novo variants in the transmembrane domain of FGFR3 on the same allele: A case report. Molecular genetics & genomic medicine. 8 (3), p. n/a. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Nagata, T. et al. (2020). Severe achondroplasia due to two de novo variants in the transmembrane domain of FGFR3 on the same allele: A case report. Molecular genetics & genomic medicine. 8 (3), p. n/a. [Online].