Turn on more accessible mode

Turn off more accessible mode

Skip Ribbon Commands

Skip to main content

Turn off Animations

Turn on Animations

Back To Search Results

Dr Goh Lay Kuan Jeannette

Dr Goh Lay Kuan Jeannette

MBBS (UK), BSc (Medical Sciences with Medical Genetics) (UK), Master of Medicine (Paediatric Medicine), MMed (Paeds) (Spore), Membership of Paediatrics and Child Health, MRCPCH (UK)

Consultant

KK Women's and Children's Hospital

Specialty: Genetics Service

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 SingHealth Duke-NUS Genomic Medicine Centre
Consultant Genetics Service KK Women's and Children's Hospital

Profile

Education

MBBS (UK)
Bsc (Medical Genetics) (UK)
MMed (Paeds) (Spore)
MRCPCH (Paeds) (UK)

Professional Appointments and Committee Memberships

Consultant, Department of Paediatrics, Genetics Service

Awards

Research Interests

Publications

Research Trials

Tags: Genetics Service, 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