D. Lam

发表

Molecular characterization of the developmental gene in eyes: through data-mining on integrated transcriptome databases.

T. Gojobori, K. Ikeo, K. Choy, 2006, Clinical biochemistry.

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

K. Choy, Y. Leung, C. Pang, 2000, Investigative ophthalmology & visual science.

A novel missense RP1 mutation in retinitis pigmentosa

C. Pang, D. Lam, K. Chong, 2006, Eye.

When drugs development meets genomics

Y. Leung, C. Pang, D. Lam, 2001, The Pharmacogenomics Journal.

Gene mutations in retinitis pigmentosa and their clinical implications.

C. Pang, B. Fan, L. Baum, 2005, Clinica chimica acta; international journal of clinical chemistry.

Absence of trabecular meshwork-inducible stretch response (TISR)/oculomedin gene and proximal promoter mutation in primary open angle glaucoma patients

Y. Leung, C. Pang, L. Baum, 2000, Human Genetics.

Indocyanine green staining and removal of internal limiting membrane in macular hole surgery: histology and outcome.

T. Lai, D. Lam, G. Yam, 2001, American journal of ophthalmology.

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

Y. Leung, C. Pang, L. Baum, 1999, Human mutation.

An in vitro study on the compatibility and precipitation of a combination of ciprofloxacin and vancomycin in human vitreous

C. Pang, D. Lam, S. Cheung, 2004, British Journal of Ophthalmology.

Molecular diagnostics for retinitis pigmentosa.

C. Pang, L. Baum, D. Lam, 2001, Clinica chimica acta; international journal of clinical chemistry.

Genomic annotation of 15,809 ESTs identified from pooled early gestation human eyes.

T. Gojobori, K. Ikeo, K. Choy, 2006, Physiological genomics.

Genetic markers for retinitis pigmentosa.

C. Pang, D. Lam, P. O. Tam, 2005, Hong Kong medical journal = Xianggang yi xue za zhi.

Novel TIGR sequence alteration Val53Ala

Y. Leung, L. Baum, D. Lam, 2000, Human mutation.

High-throughput conformation-sensitive gel electrophoresis for discovery of SNPs.

K. Choy, Y. Leung, C. Pang, 2001, BioTechniques.

Loss of heterozygosity and mutations are the major mechanisms of RB1 gene inactivation in Chinese with sporadic retinoblastoma

K. Choy, C. Pang, D. Lam, 2002, Human mutation.

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

C. Pang, L. Baum, D. Lam, 2001, Human mutation.

An in vitro study on the compatibility and concentrations of combinations of vancomycin, amikacin, and dexamethasone in human vitreous

C. Pang, D. Lam, S. Cheung, 2007, Eye.

Cost savings using automated DNA sequencing.

Y. Leung, C. Pang, L. Baum, 2000, BioTechniques.

A novel mutation in CRYBB2 responsible for inherited coronary cataract

C. Pang, D. Lam, D. Lam, 2009, Eye.