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机译:ENG基因中的等位基因缺失,影响遗传性出血性毛细血管扩张的基因检测结果
Departments of Clinical Genetics and Odense University Hospital, University of Southern Denmark, Odense C,Denmark,Departments of Otorhinolaryngology, Odense University Hospital, University of Southern Denmark, Odense C,Denmark,Department of Clinical Genetics Odense University Hospital University of Southern Denmark Sdr. Boulevard 29 DK-5000 Odense C Denmark;
Departments of Otorhinolaryngology, Odense University Hospital, University of Southern Denmark, Odense C,Denmark;
Departments of Clinical Genetics and Odense University Hospital, University of Southern Denmark, Odense C,Denmark;
Departments of Clinical Genetics and Odense University Hospital, University of Southern Denmark, Odense C,Denmark;
Departments of Clinical Genetics and Odense University Hospital, University of Southern Denmark, Odense C,Denmark;
机译:ENG和ACVRL1的新突变是在200名接受遗传性出血性毛细血管扩张(HHT)临床基因测试的个体中发现的:基因型与表型的相关性。
机译:评论基因专利和许可实践对获得基因检测的影响:遗传性出血性毛细血管扩张的教训。
机译:遗传性出血性毛细血管梭中的组织特异性镶嵌:对家庭遗传检测的影响
机译:临床干细胞疗法:脑内出血中遗传工程化间充质干细胞的脑移植脑内出血中的神经保护和神经元
机译:“美国乳房外科医生2019年围攻指南对遗传乳腺癌遗传检测”的影响癌症遗传咨询师
机译:遗传性出血性毛细血管扩张的血管畸形的体细胞突变导致ENG或ACVRL1的双等位基因丢失
机译:遗传性出血性毛细管扩张患者的常见和独特致病特征1和遗传性出血性毛细管扩张患者2动物模型简报