Cita APA

Wade, E. M., Parthasarathy, P., Mi, J., Morgan, T., Wollnik, B., Robertson, S. P., & Cundy, T. (2021). Deletion of the last two exons of FGF10 in a family with LADD syndrome and pulmonary acinar hypoplasia. Eur J Hum Genet.

Chicago Style Citation

Wade, Emma M., Padmini Parthasarathy, Jingyi Mi, Tim Morgan, Bernd Wollnik, Stephen P. Robertson, i Tim Cundy. "Deletion of the Last Two Exons of FGF10 in a Family With LADD Syndrome and Pulmonary Acinar Hypoplasia." Eur J Hum Genet 2021.

Cita MLA

Wade, Emma M., et al. "Deletion of the Last Two Exons of FGF10 in a Family With LADD Syndrome and Pulmonary Acinar Hypoplasia." Eur J Hum Genet 2021.