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Naseer, M. I.; Rasool, M.; Abdulkareem, A. A.; Chaudhary, A. G.; Zaidi, S. K.; Al-Qahtani, M. H. 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 2019, 35.