机译:常规PCR方法快速检测MECP2热点C末端区段中的缺失:两名印度裔经典Rett综合征患者的报告
Genetics Unit, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India;
Genetics Unit, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India;
Genetics Unit, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India;
Genetics Unit, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India;
Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India;
Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India;
Genetics Unit, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India Genetics Unit Department of Pediatrics AH India Institute of Medical Sciences New Delhi 110029 India;
机译:突尼斯rett综合征患者MECP2基因C末端区域的新突变
机译:更新Rett综合征中C端MECP2缺失的概况。
机译:印度Rett综合征患者队列中MECP2基因突变的光谱:两个新突变的报告
机译:更新C末端缺失mECp2在Rett综合征轮廓
机译:通过鲁棒剂量PCR(RD-PCR)检测rett综合征中MECP2基因的杂合缺失和重复