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Molecular basis of von Hippel-Lindau syndrome in Chinese patients.
Siu WK, Ma RC, Lam CW, Mak CM, Yuen YP, Lo FM, Chan KW, Lam SF, Ling SC, Tong SF, So WY, Chow CC, Tang MH, Tam WH, Chan AY. Siu WK, et al. Among authors: mak cm. Chin Med J (Engl). 2011 Jan;124(2):237-41. Chin Med J (Engl). 2011. PMID: 21362373
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: identification of 17 novel mutations and its genetic heterogeneity.
Mak CM, Lam CW, Tam S, Lai CL, Chan LY, Fan ST, Lau YL, Lai JY, Yuen P, Hui J, Fu CC, Wong KS, Mak WL, Tze K, Tong SF, Lau A, Leung N, Hui A, Cheung KM, Ko CH, Chan YK, Ma O, Chau TN, Chiu A, Chan YW. Mak CM, et al. Among authors: mak wl. J Hum Genet. 2008;53(1):55-63. doi: 10.1007/s10038-007-0218-2. Epub 2007 Nov 22. J Hum Genet. 2008. PMID: 18034201
133 results