Mullin HC Yu

Rapid whole-exome sequencing facilitates precision medicine in paediatric rare disease patients and reduces healthcare costs

Y. Lau, B. Chung, M. Chan, 2020, The Lancet regional health. Western Pacific.

Whole exome sequencing for prenatal diagnosis of CHARGE syndrome: a case report

B. Chung, W. To, C. Kong, 2019, Hong Kong Journal of Gynaecology, Obstetrics and Midwifery.

Megaconial congenital muscular dystrophy: Same novel homozygous mutation in CHKB gene in two unrelated Chinese patients

B. Chung, P. Khong, M. Yeung, 2019, Neuromuscular Disorders.