APA (7th ed.) Citation

Moey, L. H., Seo, G. H., Cheah, B. E., Keng, W. T., Lee, H., & Ch’ng, G. S. (2025). A first large study of whole-exome sequencing (WES) in 489 patients with suspected rare genetic disorders at a tertiary centre in Malaysia. Elsevier.

Chicago Style (17th ed.) Citation

Moey, Lip Hen, Go Hun Seo, Boon Eu Cheah, Wee Teik Keng, Hane Lee, and Gaik Siew Ch’ng. A First Large Study of Whole-exome Sequencing (WES) in 489 Patients with Suspected Rare Genetic Disorders at a Tertiary Centre in Malaysia. Elsevier, 2025.

MLA (9th ed.) Citation

Moey, Lip Hen, et al. A First Large Study of Whole-exome Sequencing (WES) in 489 Patients with Suspected Rare Genetic Disorders at a Tertiary Centre in Malaysia. Elsevier, 2025.