机译:染色体常染色体隐性非综合征性听觉障碍的新位点DFNB63映射到染色体11q13.2–q13.4
Department of Human Genetics Radboud University Nijmegen Medical Centre Nijmegen The Netherlands;
Department of Otorhinolaryngology Faculty of Medicine Karadeniz Technical University Trabzon Turkey;
Department of Otorhinolaryngology Faculty of Medicine Yuzuncu Yil University Van Turkey;
Department of Ophthalmology Faculty of Medicine Yuzuncu Yil University Van Turkey;
Department of Otorhinolaryngology Radboud University Nijmegen Medical Centre Nijmegen The Netherlands;
Department of Human Genetics Radboud University Nijmegen Medical Centre Nijmegen The Netherlands;
Department of Otorhinolaryngology Radboud University Nijmegen Medical Centre Nijmegen The Netherlands;
Department of Otorhinolaryngology Radboud University Nijmegen Medical Centre Nijmegen The Netherlands;
Department of Human Genetics Radboud University Nijmegen Medical Centre Nijmegen The Netherlands;
Department of Medical Biology and Genetics Faculty of Medicine Karadeniz Technical University Trabzon Turkey;
Department of Otorhinolaryngology Radboud University Nijmegen Medical Centre Nijmegen The Netherlands;
ARNSHI; DFNB63; Deafness; Hearing loss; 11q13.2–q13.4;
机译:染色体常染色体隐性非综合征性听觉障碍的新位点DFNB63映射到染色体11q13.2-q13.4。
机译:染色体11q13.2–q13.3的常染色体隐性非综合征性耳聋位点DFNB63
机译:一个新颖的常染色体隐性非综合征性听力障碍基因座(DFNB42)映射到染色体3q13.31-q22.3。
机译:全基因组连杆和单倍型关联研究在染色体7中映射颅内动脉瘤至弹性蛋白基因座
机译:在17q25上绘制一个新的常染色体显性遗传性听力损失基因座DFNA20,并寻找引起疾病的基因。
机译:新型常染色体隐性非综合征性听力障碍(DFNB42)映射到染色体3q13.31-q22.3。
机译:一种新型常血糖隐性不合因的非yndromic听力障碍基因座(DFNB42)映射到染色体3Q13.31-Q22.3