Szymońska, I., Borgenvik, T. L., Karlsvik, T. M., Halsen, A., Malecki, B. K., Saetre, S. E., . . . Malecki, M. (2015). Novel mutation-deletion in the PHOX2B gene of the patient diagnosed with Neuroblastoma, Hirschsprung’s Disease, and Congenital Central Hypoventilation Syndrome (NB-HSCR-CCHS) Cluster. J Genet Syndr Gene Ther.
Chicago Style CitationSzymońska, Izabela, et al. "Novel Mutation-deletion in the PHOX2B Gene of the Patient Diagnosed With Neuroblastoma, Hirschsprung’s Disease, and Congenital Central Hypoventilation Syndrome (NB-HSCR-CCHS) Cluster." J Genet Syndr Gene Ther 2015.
Cita MLASzymońska, Izabela, et al. "Novel Mutation-deletion in the PHOX2B Gene of the Patient Diagnosed With Neuroblastoma, Hirschsprung’s Disease, and Congenital Central Hypoventilation Syndrome (NB-HSCR-CCHS) Cluster." J Genet Syndr Gene Ther 2015.