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Department Of Paediatrics Prince Of Wales Hospital The Chinese University Of Hong Kong Hong Kong Spe | 論文
- Mutational and haplotype analysis of AGL in patients with glycogen storage disease type III
- Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese : Identification of 17 novel mutations and its genetic heterogeneity
- Galactorrhea : A strong clinical clue towards the diagnosis of neurotransmitter disease
- First report of GLUT1 deficiency syndrome in Chinese patients with novel and hot spot mutations in SLC2A1 gene