Cite
A respiratory/Hirschsprung phenotype in a three-generation family associated with a novel pathogenic PHOX2B splice donor mutation.
MLA
Pace, Nikolai Paul, et al. “A Respiratory/Hirschsprung Phenotype in a Three-Generation Family Associated with a Novel Pathogenic PHOX2B Splice Donor Mutation.” Molecular Genetics & Genomic Medicine, vol. 8, no. 12, Dec. 2020, p. e1528. EBSCOhost, https://doi.org/10.1002/mgg3.1528.
APA
Pace, N. P., Pace Bardon, M., & Borg, I. (2020). A respiratory/Hirschsprung phenotype in a three-generation family associated with a novel pathogenic PHOX2B splice donor mutation. Molecular Genetics & Genomic Medicine, 8(12), e1528. https://doi.org/10.1002/mgg3.1528
Chicago
Pace, Nikolai Paul, Michael Pace Bardon, and Isabella Borg. 2020. “A Respiratory/Hirschsprung Phenotype in a Three-Generation Family Associated with a Novel Pathogenic PHOX2B Splice Donor Mutation.” Molecular Genetics & Genomic Medicine 8 (12): e1528. doi:10.1002/mgg3.1528.