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Page 1
SPP2 Mutations Cause Autosomal Dominant Retinitis Pigmentosa.
Liu Y, Chen X, Xu Q, Gao X, Tam PO, Zhao K, Zhang X, Chen LJ, Jia W, Zhao Q, Vollrath D, Pang CP, Zhao C. Liu Y, et al. Among authors: tam po. Sci Rep. 2015 Oct 13;5:14867. doi: 10.1038/srep14867. Sci Rep. 2015. PMID: 26459573 Free PMC article.
Familial high myopia linkage to chromosome 18p.
Lam DS, Tam PO, Fan DS, Baum L, Leung YF, Pang CP. Lam DS, et al. Among authors: tam po. Ophthalmologica. 2003 Mar-Apr;217(2):115-8. doi: 10.1159/000068554. Ophthalmologica. 2003. PMID: 12592049
Different optineurin mutation pattern in primary open-angle glaucoma.
Leung YF, Fan BJ, Lam DS, Lee WS, Tam PO, Chua JK, Tham CC, Lai JS, Fan DS, Pang CP. Leung YF, et al. Among authors: tam po. Invest Ophthalmol Vis Sci. 2003 Sep;44(9):3880-4. doi: 10.1167/iovs.02-0693. Invest Ophthalmol Vis Sci. 2003. PMID: 12939304
A novel missense RP1 mutation in retinitis pigmentosa.
Chiang SW, Wang DY, Chan WM, Tam PO, Chong KK, Lam DS, Pang CP. Chiang SW, et al. Among authors: tam po. Eye (Lond). 2006 May;20(5):602-5. doi: 10.1038/sj.eye.6701944. Eye (Lond). 2006. PMID: 15933747 Review.
Genetic markers for retinitis pigmentosa.
Wang DY, Chan WM, Tam PO, Chiang SW, Lam DS, Chong KK, Pang CP. Wang DY, et al. Among authors: tam po. Hong Kong Med J. 2005 Aug;11(4):281-8. Hong Kong Med J. 2005. PMID: 16085945 Free article. Review.
107 results