NASEER, Muhammad Imran; RASOOL, Mahmood; ABDULKAREEM, Angham Abdulrahman; CHAUDHARY, Adeel G.; ZAIDI, Syed Kashif; AL-QAHTANI, Mohammad 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. Pakistan Journal of Medical Sciences, [S. l.], v. 35, n. 3, 2019. DOI: 10.12669/pjms.35.3.36. Disponível em: https://pjms.org.pk/index.php/pjms/article/view/36. Acesso em: 16 jun. 2026.