Micheal, S., Siddiqui, S. N., Zafar, S. N., Venselaar, H., Qamar, R., Khan, M. I., & den Hollander, A. I. (2015). Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld–Rieger syndrome. Neurogenetics.

Micheal, Shazia, Sorath Noorani Siddiqui, Saemah Nuzhat Zafar, Hanka Venselaar, Raheel Qamar, Muhammad Imran Khan, und Anneke I. den Hollander. "Whole Exome Sequencing Identifies a Heterozygous Missense Variant in the PRDM5 Gene in a Family With Axenfeld–Rieger Syndrome." Neurogenetics 2015.

Micheal, Shazia, et al. "Whole Exome Sequencing Identifies a Heterozygous Missense Variant in the PRDM5 Gene in a Family With Axenfeld–Rieger Syndrome." Neurogenetics 2015.