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Results: 1-25/27
Authors:
Lam, CW
Arlt, W
Chan, CK
Honour, JW
Lin, CJ
Tong, SF
Choy, KW
Miller, WL
Citation: Cw. Lam et al., Mutation of proline 409 to arginine in the meander region of cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency, MOL GEN MET, 72(3), 2001, pp. 254-259
Authors:
Ko, CH
Lam, CW
Tse, PWT
Kong, CK
Chan, AKH
Wong, LJC
Citation: Ch. Ko et al., De novo mutation in the mitochondrial tRNA(Leu(UUR)) gene (A3243G) with rapid segregation resulting in MELAS in the offspring, J PAEDIAT C, 37(1), 2001, pp. 87-90
Authors:
Chow, KM
Hui, CF
Lam, CW
Morgan, RR
Whatley, SD
Richard, K
Wong, KS
Citation: Km. Chow et al., Clinical and genetic features of variegate porphyria in a Chinese patient, CHIN MED J, 114(4), 2001, pp. 424-427
Authors:
Lam, CW
Yuen, YP
Lai, CK
Tong, SF
Lau, LK
Tong, KL
Chan, YW
Citation: Cw. Lam et al., Novel mutation in the GRHPR gene in a Chinese patient with primary hyperoxaluria type 2 requiring renal transplantation from a living related donor, AM J KIDNEY, 38(6), 2001, pp. 1307-1310
Authors:
Lam, CW
Poon, PMK
Tong, SF
Ko, CH
Citation: Cw. Lam et al., Two novel CLN2 gene mutations in a Chinese patient with classical late-infantile neuronal ceroid lipofuscinosis, AM J MED G, 99(2), 2001, pp. 161-163
Authors:
Orrico, A
Galli, L
Zappella, M
Lam, CW
Bonifacio, S
Torricelli, F
Hayek, G
Citation: A. Orrico et al., Possible case of Pitt-Hopkins syndrome in sibs, AM J MED G, 103(2), 2001, pp. 157-159
Authors:
Lam, CW
Citation: Cw. Lam, Comparing the social policy experience of Britain and Taiwan, SOC POL ADM, 35(3), 2001, pp. 341-342
Authors:
Kong, CK
Ko, CH
Tong, SF
Lam, CW
Citation: Ck. Kong et al., Atypical presentation of dopa-responsive dystonia: Generalized hypotonia and proximal weakness, NEUROLOGY, 57(6), 2001, pp. 1121-1124
Authors:
Lam, CW
Chen, ML
Citation: Cw. Lam et Ml. Chen, Pleural protein capillary electrophoresis for the separation of transudates and exudates - Response, CLIN CHEM, 47(5), 2001, pp. 976-976
Authors:
Lam, CW
Poon, PMK
Tong, SF
Lo, AWI
Lai, CK
Choi, KL
Tiu, SC
Chan, YW
Shek, CC
Citation: Cw. Lam et al., Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC, CLIN CHEM, 47(2), 2001, pp. 343-346
Authors:
Lam, CW
Hui, KN
Poon, PMK
Luk, NM
Yuen, YP
Tong, SF
Lai, CK
Chan, YW
Lo, KK
Citation: Cw. Lam et al., Novel splicing mutation of the PPOX gene (IVS10+1G -> A) detected by denaturing high-performance liquid chromatography, CLIN CHIM A, 305(1-2), 2001, pp. 197-200
Authors:
Lam, CW
Mak, YT
Lo, YMD
Tong, SF
To, KF
Lai, FMM
Citation: Cw. Lam et al., Molecular genetic analysis of a Chinese patient with Fabry disease, CHIN MED J, 113(2), 2000, pp. 186-188
Authors:
Sirgel, FA
Donald, PR
Odhiambo, J
Githui, W
Umapathy, KC
Paramasivan, CN
Tam, CM
Kam, KM
Lam, CW
Sole, KM
Mitchison, DA
Citation: Fa. Sirgel et al., A multicentre study of the early bactericidal activity of anti-tuberculosis drugs, J ANTIMICRO, 45(6), 2000, pp. 859-870
Authors:
Lee, V
Li, CK
Shing, MMK
Chik, KW
Lam, CW
Tsang, KS
Pong, H
Huen, KF
Yuen, PMP
Citation: V. Lee et al., Umbilical cord blood transplantation for Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI), BONE MAR TR, 26(4), 2000, pp. 455-458
Authors:
Lam, CW
Citation: Cw. Lam, Enumeration of isomers of alkylcyclopropanes by means of alkyl 1,1-biradicals, J MATH CHEM, 27(1-2), 2000, pp. 23-25
Authors:
Lam, CW
Sin, SY
Lau, ET
Lam, YY
Poon, P
Tong, SF
Citation: Cw. Lam et al., Prenatal diagnosis of glycogen storage disease type 1b using denaturing high performance liquid chromatography, PRENAT DIAG, 20(9), 2000, pp. 765-768
Authors:
Mercero, JM
Barrett, P
Lam, CW
Fowler, JE
Ugalde, JM
Pedersen, LG
Citation: Jm. Mercero et al., Quantum mechanical calculations on phosphate hydrolysis reactions, J COMPUT CH, 21(1), 2000, pp. 43-51
Authors:
Orrico, A
Lam, CW
Galli, L
Dotti, MT
Hayek, G
Tong, SF
Poon, PMK
Zappella, M
Federico, A
Sorrentino, V
Citation: A. Orrico et al., MECP2 mutation in male patients with non-specific X-linked mental retardation, FEBS LETTER, 481(3), 2000, pp. 285-288
Authors:
Lo, YMD
Chan, ATC
Chan, LYS
Leung, SF
Lam, CW
Huang, DP
Johnson, PJ
Citation: Ymd. Lo et al., Molecular prognostication of nasopharyngeal carcinoma by quantitative analysis of circulating Epstein-Barr virus DNA, CANCER RES, 60(24), 2000, pp. 6878-6881
Authors:
Au, WY
Tam, SCF
Ho, KM
Lam, CW
Kwong, YL
Citation: Wy. Au et al., Hypertrichosis due to porphyria cutanea tarda associated with blastic transformation of myelofibrosis (vol 141, pg 932, 1999), BR J DERM, 142(3), 2000, pp. 628-628
Authors:
Lam, CW
Xie, JW
To, KF
Ng, HK
Lee, KC
Yuen, NWF
Lim, PL
Chan, LYS
Tong, SF
McCormick, F
Citation: Cw. Lam et al., A frequent activated smoothened mutation in sporadic basal cell carcinomas, ONCOGENE, 18(3), 1999, pp. 833-836
Authors:
Lam, CW
Wilson, PR
Citation: Cw. Lam et Pr. Wilson, Crown cementation and pulpal health, INT ENDOD J, 32(4), 1999, pp. 249-256
Authors:
Lam, CW
Citation: Cw. Lam, Origin of the Japanese population, SCIENCE, 284(5417), 1999, pp. 1125-1125
Authors:
Galli, L
Orrico, A
Marcolongo, P
Fulceri, R
Burchell, A
Melis, D
Parini, R
Gatti, R
Lam, CW
Benedetti, A
Sorrentino, V
Citation: L. Galli et al., Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c, FEBS LETTER, 459(2), 1999, pp. 255-258
Authors:
Lam, CW
Chan, BY
Tong, SF
Citation: Cw. Lam et al., Definition of the correct sequence in the donor splice site of intron 2 inthe human glucose 6-phosphate translocase gene, FEBS LETTER, 445(2-3), 1999, pp. 449-450