Citação norma APA

Kumar, R. A., Everman, D. B., Morgan, C. T., Slavotinek, A., Schwartz, C. E., & Simpson, E. M. (2007). Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes. BioMed Central.

Citação norma Chicago

Kumar, Ravinesh A., David B. Everman, Chad T. Morgan, Anne Slavotinek, Charles E. Schwartz, and Elizabeth M. Simpson. Absence of Mutations in NR2E1 and SNX3 in Five Patients With MMEP (microcephaly, Microphthalmia, Ectrodactyly, and Prognathism) and Related Phenotypes. BioMed Central, 2007.

Citação norma MLA

Kumar, Ravinesh A., et al. Absence of Mutations in NR2E1 and SNX3 in Five Patients With MMEP (microcephaly, Microphthalmia, Ectrodactyly, and Prognathism) and Related Phenotypes. BioMed Central, 2007.

Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.