AWAN, M. Q. Clinical Utility of Whole Genome Sequencing for Undiagnosed Rare Genetic Disorders. Journal of Liaquat University of Medical & Health Sciences, [S. l.], v. 20, n. 01, p. 1–2, 2021. Disponível em: http://121.52.154.205/index.php/jlumhs/article/view/590. Acesso em: 15 nov. 2024.