Dr Koh Ai Ling

MB ChB (Edinburgh, UK), MRCPCH (RCPCH, UK), M Med (Paed) (Spore)

Consultant

KK Women's and Children's Hospital

Specialty: Paediatric Genetics

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Education and Training

Publications

Conditions Treated By This Doctor

22q11.2 Deletion Syndrome Achondroplasia Citrin Deficiency Inherited Retinal Diseases Klinefelter Syndrome Medium-Chain Acyl-CoA Dehydrogenase Deficiency Mitochondrial Diseases Triple X Syndrome Turner Syndrome

Clinical Appointments

Clinical Lead, Paediatrics
Therapeutics Lead

SingHealth Duke-NUS Genomic Medicine Centre

Consultant

Genetics Service

Education and Training

MB ChB (U of Edinburgh, United Kingdom) 2009
MRCPCH (RCPCH, United Kingdom) 2016
M Med (Paed) (NUS, Singapore) 2016

Publications

Koh AL, Tan ES, Brett MS, Lai AH, Jamuar SS, Ng I, Tan EC. The spectrum of genetic variants and phenotypic features of Southeast Asian patients with Noonan syndrome. Molecular genetics & genomic medicine. 2019 Feb 19:e581.
B McNeills, R James, AL Koh, T Sparkes, S Shantikumar. (2011). Get Ahead! Medicine: 300 SBAs for Finals. Hodder Education, London, UK