Micheal, S., Siddiqui, S. N., Zafar, S. N., Villanueva-Mendoza, C., Cortés-González, V., Khan, M. I., & den Hollander, A. I. (2016). A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma. PLoS One.
Chicago ZitierstilMicheal, Shazia, Sorath Noorani Siddiqui, Saemah Nuzhat Zafar, Cristina Villanueva-Mendoza, Vianney Cortés-González, Muhammad Imran Khan, und Anneke I. den Hollander. "A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome With Congenital Glaucoma." PLoS One 2016.
MLA ZitierstilMicheal, Shazia, et al. "A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome With Congenital Glaucoma." PLoS One 2016.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.