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    A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Chinese patients

    A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Chinese patients by Wang Zhiqing, Chen Yulan, Wu Baoping, Zheng Haoxuan, He Jiman, Jiang Bo

    Published 2011-12-01
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