Lam DS - Search Results

1

Congenital hypertrophy of the retinal pigment epithelium and APC mutations in Chinese with familial adenomatous polyposis.

Pang CP, Fan DS, Keung JW, Baum L, Tang NL, Lau JW, Lam DS. Pang CP, et al. Among authors: lam ds. Ophthalmologica. 2001 Nov-Dec;215(6):408-11. doi: 10.1159/000050898. Ophthalmologica. 2001. PMID: 11741105

2

Differential occurrence of mutations causative of eye diseases in the Chinese population.

Pang CP, Lam DS. Pang CP, et al. Among authors: lam ds. Hum Mutat. 2002 Mar;19(3):189-208. doi: 10.1002/humu.10053. Hum Mutat. 2002. PMID: 11857735 Review.

3

Incidence and predictive value of congenital hypertrophy of retinal pigment epithelium in Chinese familial adenomatous polyposis patients.

Lam DS, Kwok SP, Kwok AK, Liew CT, Lau JW, Pang CC. Lam DS, et al. Chin Med J (Engl). 1998 Mar;111(3):278-81. Chin Med J (Engl). 1998. PMID: 10374435

4

Congenital hypertrophy of the retinal pigment epithelium and APC mutations in two Chinese families with familial adenomatous polyposis.

Pang CP, Keung JW, Tang NL, Fan DS, Lau JW, Lam DS. Pang CP, et al. Among authors: lam ds. Eye (Lond). 2000 Feb;14 ( Pt 1):18-22. doi: 10.1038/eye.2000.5. Eye (Lond). 2000. PMID: 10755094

5

Truncations in the TIGR gene in individuals with and without primary open-angle glaucoma.

Lam DS, Leung YF, Chua JK, Baum L, Fan DS, Choy KW, Pang CP. Lam DS, et al. Invest Ophthalmol Vis Sci. 2000 May;41(6):1386-91. Invest Ophthalmol Vis Sci. 2000. PMID: 10798654

6

The apolipoprotein E epsilon4 allele is unlikely to be a major risk factor of age-related macular degeneration in Chinese.

Pang CP, Baum L, Chan WM, Lau TC, Poon PM, Lam DS. Pang CP, et al. Among authors: lam ds. Ophthalmologica. 2000;214(4):289-91. doi: 10.1159/000027506. Ophthalmologica. 2000. PMID: 10859513

7

RP1 in Chinese: Eight novel variants and evidence that truncation of the extreme C-terminal does not cause retinitis pigmentosa.

Baum L, Chan WM, Yeung KY, Lam DS, Kwok AK, Pang CP. Baum L, et al. Among authors: lam ds. Hum Mutat. 2001 May;17(5):436. doi: 10.1002/humu.1127. Hum Mutat. 2001. PMID: 11317367

8

Rhodopsin mutations in Chinese patients with retinitis pigmentosa.

Chan WM, Yeung KY, Pang CP, Baum L, Lau TC, Kwok AK, Lam DS. Chan WM, et al. Among authors: lam ds. Br J Ophthalmol. 2001 Sep;85(9):1046-8. doi: 10.1136/bjo.85.9.1046. Br J Ophthalmol. 2001. PMID: 11520753 Free PMC article.

9

TGFbeta-induced factor: a candidate gene for high myopia.

Lam DS, Lee WS, Leung YF, Tam PO, Fan DS, Fan BJ, Pang CP. Lam DS, et al. Invest Ophthalmol Vis Sci. 2003 Mar;44(3):1012-5. doi: 10.1167/iovs.02-0058. Invest Ophthalmol Vis Sci. 2003. PMID: 12601022

10

A novel deletion variant of gammaD-crystallin responsible for congenital nuclear cataract.

Zhang LY, Yam GH, Fan DS, Tam PO, Lam DS, Pang CP. Zhang LY, et al. Among authors: lam ds. Mol Vis. 2007 Nov 7;13:2096-104. Mol Vis. 2007. PMID: 18079686

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