Kin Shing Lun

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

Claudia Ching Yan Chung, Gordon K. C. Leung, Christopher Chun Yu Mak et al. · The Lancet Regional Health - Western Pacific · 2020 · 68 citations · Full text

Life Sciences, Genetics, Pediatrics +17

Achieving biventricular circulation in patients with moderate hypoplastic right ventricle in pulmonary atresia intact ventricular septum after transcatheter pulmonary valve perforation

Robin Hay-Son Chen, Adolphus Kai-tung Chau, Pak‐cheong Chow et al. · Congenital Heart Disease · 2018 · 19 citations

Medicine, Cardiology, Surgery +11

A newborn with a 790 kb chromosome 17p13.3 microduplication presenting with aortic stenosis, microcephaly and dysmorphic facial features – Is cardiac assessment necessary for all patients with 17p13.3 microduplication?

Alvin Chi Chung Ho, Anthony P. Y. Liu, Kin Shing Lun et al. · European Journal of Medical Genetics · 2012 · 16 citations

Medicine, Genetics, Molecular Genetics +17