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Decapitated in vitro plantlets \nwere used as explants. Shoot etiolation was induced by placing \nexplants in a Murashige and Skoog (MS) medium containing NAA (10 \nmu M) and incubating in darkness at 28C for30 to 40 days. The \nmean number of the regenerated etiolated shoots per explant was \n2.6+/-0.29. The etiolated shoots were placed into N6 medium \nsupplemented with kinetin or BA (25 or 20 mu M, respectively). \nAfter 4 to 6 weeks, shoots regenerated along the nodes. The \nhighest regeneration rate was 15 and 13 plantlets per node with \n25 mu M kinetin and 20 mu M BA, respectively. Regenerated \nplantlets were rooted on a growth-regulator-free MS medium. \nResidual shoots of the initial explants could be recycled by \nrooting on a growth-regulator-free MS medium. 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