| Title | Author(s) | Year | View Count |  | Analysis of inborn errors of metabolism: Disease spectrum for expanded newborn screening in Hong Kong | Lee, HCH; Mak, CM; Lam, CW; Yuen, YP; Chen, AOK; Shek, CC; Siu, TS; Lai, CK; Ching, CK; Siu, WK; Chen, SPL; Law, CY; Tai, MHL; Tam, S; Chan, AYW | 2011 | 137 |
| Chemical pathology case conference - Serum tumour markers | Poon, WT; Yuen, YP; Mak, CM; Chan, AOK; Chan, MHM; Chiu, RWK; Lam, CW; Mak, TWL; Shek, CC; Tai, MHL; Tam, S; Chan, AYW | 2010 | 94 |
| Novel mutations in the BCHE gene in patients with no butyrylcholinesterase activity | OnKei Chan, A; Lam, CW; Tong, SF; Man Tung, C; Yung, K; Chan, YW; Au, KM; Yuen, YP; Hung, CT; Ng, KP; Shek, CC | 2005 | 69 |
| DNA-based diagnosis of thyroid hormone resistance syndrome: A novel THRB mutation associated with mild resistance to thyroid hormone | Lam, CW; Chan, AOK; Tong, SF; Shek, CC; Sau, CT | 2005 | 109 |
| Normal cord blood thyroid-stimulating hormone in a child with resistance to thyroid hormone | Chan, AOK; Lam, CW; Lo, IFM; Lam, STS; Shek, CC; Tiu, SC; Tong, SF | 2005 | 108 |
| A novel mutation, Y255X, of the ARSB gene in a Chinese family with mucopolysaccharidosis type VI | Lam, CW; Chan, AOK; Lai, CK; Chan, WH; Chan, YW; Shek, CC; Tong, SF | 2004 | 64 |
| Infants born to mothers with severe acute respiratory syndrome. | Shek, CC; Ng, PC; Fung, GP; Cheng, FW; Chan, PK; Peiris, MJ; Lee, KH; Wong, SF; Cheung, HM; Li, AM; Hon, EK; Yeung, CK; Chow, CB; Tam, JS; Chiu, MC; Fok, TF | 2003 | 117 |
| Steroid 5α-reductase 2 deficiency in two generations of a non-consaguineous Chinese family | Lee, CY; Lam, CW; Shek, CC | 2003 | 68 |
| Diagnosis of dihydropyrimidine dehydrogenase deficiency in a neonate with thymine-uraciluria | Au, KM; Lai, CK; Yuen, YP; Shek, CC; Lam, CW; Chan, AYW | 2003 | 87 |
| Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC | Lam, CW; Poon, PMK; Tong, SF; Lo, AWI; Lai, CK; Choi, KL; Tiu, SC; Chan, YW; Shek, CC | 2001 | 54 |
| Glucose-6-phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1a | Lam, CW; But, WM; Shek, CC; Tong, SF; Chan, YS; Choy, KW; Tse, WY; Pang, CP; Hjelm, NM | 1998 | 88 |
| Biochemical investigation of young hospitalized Chinese children: Results over a 7-year period | Pang, CP; Law, LK; Mak, YT; Shek, CC; Cheung, KL; Mak, TWL; Lam, CW; Chan, AYW; Fok, TF | 1997 | 79 |
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