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机译:与新生儿中的NPRL3基因变体相关的麻血性和难治性癫痫发作:案例报告
Valley Childrens Hosp Med Genet &
Metab 9300 Valley Childrens Pl Madera CA 93636 USA;
Valley Childrens Hosp Med Genet &
Metab 9300 Valley Childrens Pl Madera CA 93636 USA;
Valley Childrens Hosp Med Genet &
Metab 9300 Valley Childrens Pl Madera CA 93636 USA;
Valley Childrens Hosp Med Genet &
Metab 9300 Valley Childrens Pl Madera CA 93636 USA;
Valley Childrens Hosp Med Genet &
Metab 9300 Valley Childrens Pl Madera CA 93636 USA;
Valley Childrens Hosp Med Genet &
Metab 9300 Valley Childrens Pl Madera CA 93636 USA;
Valley Childrens Hosp Med Genet &
Metab 9300 Valley Childrens Pl Madera CA 93636 USA;
Valley Childrens Hosp Med Genet &
Metab 9300 Valley Childrens Pl Madera CA 93636 USA;
hemimegalencephaly; infantile epilepsy; infantile epileptic encepahlopathy; intractable neonatal seizures; NPRL3 gene variant; NPRL3 gene;
机译:表皮痣综合征变异伴大脑干和顽固性癫痫发作的癫痫手术
机译:表皮痣综合征变异伴半巨脑和顽固性癫痫发作的癫痫手术
机译:WWOX基因中的W44X突变导致顽固性癫痫发作和发育延迟:一例病例报告
机译:患者特异性癫痫癫痫发作检测在儿科患者中难以致密的癫痫发作
机译:在遗传癌基因中具有不确定意义的个体的医学决策,以及Chek2致病变异的人
机译:WWOX基因中的W44X突变导致顽固性癫痫发作和发育延迟:一例病例报告
机译:WWOX基因中的W44X突变导致顽固性癫痫发作和发育延迟:一例病例报告
机译:新生儿血红蛋白变异的回顾性研究