M. I. Naseer, M. Rasool, A. A. Abdulkareem, A. G. Chaudhary, S. K. Zaidi, and M. H. Al-Qahtani, “Novel compound heterozygous mutations in WDR62 gene leading to developmental delay and Primary Microcephaly in Saudi Family: A novel compound heterozygous mutation in WDR62gen”, Pak J Med Sci, vol. 35, no. 3, May 2019.