Abstract
Bloodstains of 200 unrelated Han population individuals living in southern China, 100 unrelated Zhuang population individuals from Guangxi were prepared on sterilized filter and subsequently air dried. DNA was obtained from bloodstain specimens using Chelex 100 (3). PCR amplification was performed using primers labeled with fluorescent dye (2,3). The amplified products were separated and detected using ABI Prism 310 sequencer (PEBiosystems, Foster City, CA). The data were analyzed as published previously (4-6).
Issue Section:
Research Papers
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