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"黄小丽" 2 results
以癫痫为主要表现的16p11.2末端微缺失综合征病例遗传学分析
Journal of Epilepsy
2024, 10(3): 274-277
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母源KCNQ3基因突变致自限性家族性新生儿癫痫一例
Journal of Epilepsy
2024, 10(4): 364-367
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