Cite
MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development.
MLA
Buchner, Georg, et al. “MID2, a Homologue of the Opitz Syndrome Gene MID1: Similarities in Subcellular Localization and Differences in Expression during Development.” Human Molecular Genetics, vol. 8, no. 8, Aug. 1999, p. 1397. EBSCOhost, https://doi.org/10.1093/hmg/8.8.1397.
APA
Buchner, G., Montini, E., Andolfi, G., Quaderi, N., Cainarca, S., Bassi, M. T., Ballabio, A., Meroni, G., & Franco, B. (1999). MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development. Human Molecular Genetics, 8(8), 1397. https://doi.org/10.1093/hmg/8.8.1397
Chicago
Buchner, Georg, Eugenio Montini, Grazia Andolfi, Nandita Quaderi, Silvia Cainarca, Maria Teresa Bassi, Andrea Ballabio, Germana Meroni, and Brunella Franco. 1999. “MID2, a Homologue of the Opitz Syndrome Gene MID1: Similarities in Subcellular Localization and Differences in Expression during Development.” Human Molecular Genetics 8 (8): 1397. doi:10.1093/hmg/8.8.1397.