L. Perng

发表

Mutation Analysis of the Putative Tumor Suppressor Gene PTEN/MMAC1 in Hepatocellular Carcinoma

Jan-Gowth Chang, K. Yeh, J. Chang, 2000, Cancer investigation.

Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in cervical cancer.

J. Chang, C. P. Chang, C. Tsai, 2000, Gynecologic oncology.

Mutation analysis of the PTEN/MMAC1 gene in cancers of the digestive tract.

M. Kao, T. Y. Yang, J. Chang, 1999, European journal of cancer.

Rapid molecular characterization of Hb H disease in Chinese by polymerase chain reaction

P. H. Chen, J. Chang, S. Chiou, 2005, Annals of Hematology.

Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amplification created restriction sites: five mutations account for most G6PD deficiency cases in Taiwan.

T. Tang, P. H. Chen, J. Chang, 1992, Blood.

Hb Köln [beta98(FG5)Val-->Met]: the first case found in a Chinese family.

J. Chang, K. Tsan, L. Perng, 1998, Hemoglobin.

Rapid diagnosis of beta-thalassemia mutations in Chinese by naturally and amplified created restriction sites.

P. H. Chen, J. Chang, S. Chiou, 1992, Blood.

Hb Siriraj: a G-->A substitution at codon 7 of the beta-globin chain creates an MboII cutting site.

J. Chang, C. Peng, C. Tsai, 1999, Hemoglobin.

A novel C to T substitution at nucleotide 1360 of cDNA which abolishes a natural Hha I site accounts for a new G6PD deficiency gene in Chinese.

J. Chang, S. Chiou, L. Perng, 1992, Human Molecular Genetics.

Molecular characterization of secretor type α(1,2)-fucosyltransferase gene deficiency in the Philippine population

M. Kao, J. Chang, C. Peng, 1999, Annals of Hematology.