Showing results 6 to 11 of 11
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| Title | Author(s) | Issue Date | |
|---|---|---|---|
Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience Journal:Hong Kong Medical Journal | 2018 | ||
Genetic diagnosis of severe myoclonic epilepsy of infancy (Dravet syndrome) with SCN1A mutations in the Hong Kong Chinese patients Journal:Hong Kong Medical Journal | 2011 | ||
Genetics of Apparently Sporadic Pheochromocytoma and Paraganglioma in a Chinese Population Journal:Hormone and Metabolic Research | 2015 | ||
Influences of the microsomal triglyceride transfer protein gene polymorphism on plasma lipids and lipoproteins in Southern Chinese Proceeding/Conference:International Huaxia Congress of Endocrinology, IHCE-2 | 2001 | ||
NMR-based urinalysis for rapid diagnosis of β-ureidopropionase deficiency in a patient with Dravet syndrome Journal:Clinica Chimica Acta | 2015 | ||
| 2011 |