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Results: 1-10 |
Results: 10
Detection of an intense resonance at 2.4 ppm in H-1 MR spectra of patientswith severe late-delayed, radiation-induced brain injuries
Authors: Yeung, DKW Chan, YL Leung, SF Poon, PMK Pang, CP
Citation: Dkw. Yeung et al., Detection of an intense resonance at 2.4 ppm in H-1 MR spectra of patientswith severe late-delayed, radiation-induced brain injuries, MAGN RES M, 45(6), 2001, pp. 994-1000
Two novel CLN2 gene mutations in a Chinese patient with classical late-infantile neuronal ceroid lipofuscinosis
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
Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC
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
Novel splicing mutation of the PPOX gene (IVS10+1G -> A) detected by denaturing high-performance liquid chromatography
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
Rapid analysis of CGG repeat length in the FMR1 gene
Authors: Poon, PMK Zhao, Z Wu, XQ Ni, YX Pang, CP
Citation: Pmk. Poon et al., Rapid analysis of CGG repeat length in the FMR1 gene, CLIN CH L M, 38(9), 2000, pp. 935-938
The apolipoprotein E epsilon 4 allele is unlikely to be a major risk factor of age-related macular degeneration in Chinese
Authors: Pang, CP Baum, L Chan, WM Lau, TC Poon, PMK Lam, DSC
Citation: Cp. Pang et al., The apolipoprotein E epsilon 4 allele is unlikely to be a major risk factor of age-related macular degeneration in Chinese, OPHTHALMOLA, 214(4), 2000, pp. 289-291
MECP2 mutation in male patients with non-specific X-linked mental retardation
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
Trinucleotide CGG repeat in the FMR1 gene in Chinese mentally retarded patients
Authors: Pang, CP Poon, PMK Chen, QL Lai, KYC Yin, CH Zhao, Z Zhong, N Lau, CH Lam, STS Wong, CK Brown, WT
Citation: Cp. Pang et al., Trinucleotide CGG repeat in the FMR1 gene in Chinese mentally retarded patients, AM J MED G, 84(3), 1999, pp. 179-183
FRAXAC1 and DXS548 polymorphisms in the Chinese population
Authors: Poon, PMK Pang, CP Chen, QL Zhong, N Lai, KYC Lau, CH Wong, CK Brown, WT
Citation: Pmk. Poon et al., FRAXAC1 and DXS548 polymorphisms in the Chinese population, AM J MED G, 84(3), 1999, pp. 208-213
Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma
Authors: Lo, YMD Hjelm, NM Fidler, C Sargent, IL Murphy, MF Chamberlain, PF Poon, PMK Redman, CWG Wainscoat, JS
Citation: Ymd. Lo et al., Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma, N ENG J MED, 339(24), 1998, pp. 1734-1738
Risultati: 1-10 |