Baum L - Search Results

1

Gene mutations in retinitis pigmentosa and their clinical implications.

Wang DY, Chan WM, Tam PO, Baum L, Lam DS, Chong KK, Fan BJ, Pang CP. Wang DY, et al. Among authors: baum l. Clin Chim Acta. 2005 Jan;351(1-2):5-16. doi: 10.1016/j.cccn.2004.08.004. Clin Chim Acta. 2005. PMID: 15563868 Review.

2

Hunting for disease genes in multi-functional diseases.

Pang CP, Baum L, Lam DS. Pang CP, et al. Among authors: baum l. Clin Chem Lab Med. 2000 Sep;38(9):819-25. doi: 10.1515/CCLM.2000.118. Clin Chem Lab Med. 2000. PMID: 11097334 Review.

3

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. Hum Mutat. 2001 May;17(5):436. doi: 10.1002/humu.1127. Hum Mutat. 2001. PMID: 11317367

4

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: baum l. 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.

5

Molecular diagnostics for retinitis pigmentosa.

Yeung KY, Baum L, Chan WM, Lam DS, Kwok AK, Pang CP. Yeung KY, et al. Among authors: baum l. Clin Chim Acta. 2001 Nov;313(1-2):209-15. doi: 10.1016/s0009-8981(01)00674-x. Clin Chim Acta. 2001. PMID: 11694261

6

[Single nucleotide polymorphisms of the myocilin gene in primary open-angle glaucoma patients].

Fan BJ, Leung YF, Pang CP, Baum L, Tam OS, Wang N, Lam SC. Fan BJ, et al. Among authors: baum l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Feb;21(1):70-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 14767915 Chinese.

7

ABCA4 sequence variants in Chinese patients with age-related macular degeneration or Stargardt's disease.

Baum L, Chan WM, Li WY, Lam DS, Wang PB, Pang CP. Baum L, et al. Ophthalmologica. 2003 Mar-Apr;217(2):111-4. doi: 10.1159/000068553. Ophthalmologica. 2003. PMID: 12592048

8

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: baum l. Ophthalmologica. 2003 Mar-Apr;217(2):115-8. doi: 10.1159/000068554. Ophthalmologica. 2003. PMID: 12592049

9

Run-on mutation and three novel nonsense mutations identified in the PAX6 gene in patients with aniridia.

Baum L, Pang CP, Fan DS, Poon PM, Leung YF, Chua JK, Lam DS. Baum L, et al. Hum Mutat. 1999 Sep 19;14(3):272-3. doi: 10.1002/(SICI)1098-1004(1999)14:3<272::AID-HUMU21>3.0.CO;2-V. Hum Mutat. 1999. PMID: 10477494 No abstract available.

10

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. Among authors: baum l. Invest Ophthalmol Vis Sci. 2000 May;41(6):1386-91. Invest Ophthalmol Vis Sci. 2000. PMID: 10798654

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