P. G. Lim

Mutational characterization of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Malaysia

L. Wu, A. Khoo, P. Balraj, 2013, Journal of Endocrinological Investigation.

Thyroid autoimmunity and autoimmune thyroid disease in Malaysian girls with Turner syndrome: An understudied population

L. Wu, M. Y. Jalaludin, Suhaimi Hussain, 2023, Journal of paediatrics and child health.

Biochemical evaluation of an infant with hypoglycemia resulting from a novel de novo mutation of the GLUD1 gene and hyperinsulinism-hyperammonemia syndrome

S. Ellard, S. Flanagan, K. Hussain, 2011, Journal of Pediatric Endocrinology & Metabolism (JPEM).