Simpson Elizabeth M, Schwartz Charles E, Slavotinek Anne, Morgan Chad T, Everman David B, & Kumar Ravinesh A. (2007). Absence of mutations in <it>NR2E1 </it>and <it>SNX3 </it>in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes. BMC.
Чикаго стиль цитування (17-те видання)Simpson Elizabeth M, Schwartz Charles E, Slavotinek Anne, Morgan Chad T, Everman David B, та Kumar Ravinesh A. Absence of Mutations in <it>NR2E1 </it>and <it>SNX3 </it>in Five Patients with MMEP (microcephaly, Microphthalmia, Ectrodactyly, and Prognathism) and Related Phenotypes. BMC, 2007.
Стиль цитування MLA (9-ме видання)Simpson Elizabeth M, et al. Absence of Mutations in <it>NR2E1 </it>and <it>SNX3 </it>in Five Patients with MMEP (microcephaly, Microphthalmia, Ectrodactyly, and Prognathism) and Related Phenotypes. BMC, 2007.