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MBBS, MRCPCH (UK)
Specialty: Paediatric Genetics
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.