Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
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1992 | Molecular characterization of G6PD deficiency by natural and amplification created restriction sites - Five mutations account for most G6PD deficiency cases in Taiwan | Chang, J-G.; Chiou, S-S.; Perng, L-I.; Chen, T-C.; Liu, T-C.; Lee, L-S.; Chen, P-H.; Tang, T. K. | Blood 80, 1079-1082 |