Kunwar, F., Tewari, S., & Bakshi, S. R. (2017). Apert syndrome with S252W FGFR2 mutation and characterization using Phenomizer: An Indian case report. J Oral Biol Craniofac Res.
Citação norma ChicagoKunwar, Fulesh, Shikha Tewari, and Sonal R. Bakshi. "Apert Syndrome With S252W FGFR2 Mutation and Characterization Using Phenomizer: An Indian Case Report." J Oral Biol Craniofac Res 2017.
MLA引文Kunwar, Fulesh, Shikha Tewari, and Sonal R. Bakshi. "Apert Syndrome With S252W FGFR2 Mutation and Characterization Using Phenomizer: An Indian Case Report." J Oral Biol Craniofac Res 2017.
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