机译:Hypoctional pax1突变导致常染色体隐性遗传性ootofaciocercical综合症
Institute of Human Genetics University Medical Faculty University of Cologne Kerpener Str. 34;
Institute of Human Genetics University Medical Faculty University of Cologne Kerpener Str. 34;
Institute of Human Genetics University Medical Faculty University of Cologne Kerpener Str. 34;
Department of Medical Genetics Faculty of Medicine Ege University Izmir Turkey;
Department of Medical Genetics Faculty of Medicine Ege University Izmir Turkey;
Institute of Human Genetics University Medical Faculty University of Cologne Kerpener Str. 34;
Department of Medical Genetics Faculty of Medicine Ege University Izmir Turkey;
Department of Ophthalmology Faculty of Medicine Ege University Izmir Turkey;
Institute of Human Genetics University Medical Faculty University of Cologne Kerpener Str. 34;
Department of Medical Genetics Faculty of Medicine Ege University Izmir Turkey;
Institute of Human Genetics University Medical Faculty University of Cologne Kerpener Str. 34;
机译:功能低下的PAX1突变导致常染色体隐性遗传性耳面部颈综合征
机译:Hypoctional pax1突变导致常染色体隐性遗传性ootofaciocercical综合症
机译:一种新的PAX1 PAX1 PAX1纯度术治疗otofaciociachermical综合征患者的重症综合免疫缺陷相关
机译:金毛犬常染色体隐性的IChthyosisis:PNPLA1突变等位基因在不同种群中的分布和频率
机译:在常染色体隐性遗传性视网膜炎的犬模型中,每天四个月西地那非对磷酸二酯酶6突变的杂合子载体给药的研究。
机译:以色列人群中引起常染色体隐性遗传性视网膜疾病的突变的载波频率分析
机译:错误至:Hypoctional pax1突变导致常染色体隐性遗传性oTofaciocercical综合症