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机译:在KMT2A KMT2A的新型非礼突变引起的患有Wiedemann-Steiner综合征的个体中的术语
Department of PediatricsUniversity of Tsukuba HospitalIbaraki Japan;
Department of Child HealthUniversity of TsukubaIbaraki Japan;
Department of Child HealthUniversity of TsukubaIbaraki Japan;
Department of PediatricsUniversity of Tsukuba HospitalIbaraki Japan;
Department of PediatricsUniversity of Tsukuba HospitalIbaraki Japan;
Department of PediatricsUniversity of Tsukuba HospitalIbaraki Japan;
Department of PediatricsUniversity of Tsukuba HospitalIbaraki Japan;
Department of Child HealthUniversity of TsukubaIbaraki Japan;
Department of Child HealthUniversity of TsukubaIbaraki Japan;
Department of Child HealthUniversity of TsukubaIbaraki Japan;
Department of Child HealthUniversity of TsukubaIbaraki Japan;
Center for Medical GeneticsKeio University School of MedicineTokyo Japan;
Center for Medical GeneticsKeio University School of MedicineTokyo Japan;
Center for Medical GeneticsKeio University School of MedicineTokyo Japan;
KMT2A; preaxial polydactyly; Wiedemann‐Steiner syndrome;
机译:在KMT2A KMT2A的新型非礼突变引起的患有Wiedemann-Steiner综合征的个体中的术语
机译:描绘由KMT2A突变引起的Wiedemann-Steiner综合征的临床特征
机译:KMT2A(MLL)基因中的De Novo变体在通过临床外显子组测序鉴定的两个无关个体中引起非典型Wiedemann-Steiner综合征
机译:β-肾上腺素受体阻滞剂卡维地洛在HERG N588K突变引起的短QT综合征中的作用:模拟研究
机译:KMT2A(MLL)基因中的De Novo变体在临床外显子组测序确定的两个无关个体中引起非典型Wiedemann-Steiner综合征
机译:在KMT2A中的新型非礼突变引起的Wiedemann-Steiner综合征中的个体中的术语中的静脉静脉突变。 AM J MED TEAL A. 2017年; 173A:2821-2,825“