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机译:家族性单侧前庭血小马瘤很少是由NF2 NF2基因中的遗传变异引起的
Department of Genomic MedicineManchester United Kingdom;
Department of Genomic MedicineManchester United Kingdom;
Department of Genomic MedicineManchester United Kingdom;
Department of OtolaryngologyUniversity of Manchester Manchester Academic Health Science Centre;
Department of OtolaryngologyUniversity of Manchester Manchester Academic Health Science Centre;
Department of NeuroRadiologySalford Royal NHS Foundation TrustSalford Manchester United Kingdom;
Department of OtolaryngologyAddenbrooke's Hospital CambridgeUnited Kingdom;
Department of NeurosurgerySalford Royal NHS Foundation TrustSalford Manchester United Kingdom;
Department of NeurosurgerySalford Royal NHS Foundation TrustSalford Manchester United Kingdom;
Department of NeurosurgerySalford Royal NHS Foundation TrustSalford Manchester United Kingdom;
Department of NeurologySalford Royal NHS Foundation TrustSalford Manchester United Kingdom;
Department of NeuroRadiologySalford Royal NHS Foundation TrustSalford Manchester United Kingdom;
Department of NeurosurgerySalford Royal NHS Foundation TrustSalford Manchester United Kingdom;
Department of GeneticsKaiser PermanenteFontana California U.S.A.;
Johns Hopkins HospitalBaltimore Maryland U.S.A.;
Department of Genomic MedicineManchester United Kingdom;
Unilateral; vestibular schwannoma; NF2; LZTR1; familial;
机译:家族性单侧前庭血小马瘤很少是由NF2 NF2基因中的遗传变异引起的
机译:零星前庭施瓦马瘤的下一代测序:双层NF2的必要性灭活和辅助非NF2变体的影响
机译:多个单侧前庭Schwannomas:节段性NF2或零星发生?
机译:Sarcomere蛋白质基因突变和遗传性心脏病:β-心肌肌苷重链突变导致心内膜肌肌瘤和心力衰竭
机译:斑马鱼早期发育阶段人染色体22 NF2区与人类直系同源基因基因表达谱的比较
机译:家族性单侧前庭神经鞘瘤很少是由NF2基因的遗传变异引起的
机译:青年单侧前庭神经鞘瘤患者NF2基因的分子遗传学分析
机译:神经纤维瘤病2型(NF2)前庭神经鞘瘤的自然史