Search Results - Zhang, Shilin, M.D

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    The KAL1 pVal610Ile mutation is a recessive mutation causing Kallmann syndrome

    The KAL1 pVal610Ile mutation is a recessive mutation causing Kallmann syndrome by Zhang, Shilin, M.D, Xu, Hao, M.S, Wang, Tao, M.D, Liu, Guoqing, M.D, Liu, Jihong, M.D

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