机译:新型FoxF1深入内肠缺失导致致命肺部发育障碍,肺泡毛细血管发育不良,具有未对准的肺静脉
Department of Molecular and Human Genetics Baylor College of Medicine Houston TX United States;
Department of Molecular and Human Genetics Baylor College of Medicine Houston TX United States;
Department of Pediatrics Yale University School of Medicine New Haven CT United States;
Department of Pediatrics Yale University School of Medicine New Haven CT United States;
Department of Pathology Yale University School of Medicine New Haven CT United States;
Department of Pathology Baylor College of Medicine and Pulmonary Pathology Texas Children's;
Department of Molecular and Human Genetics Baylor College of Medicine Houston TX United States;
CNV; Enhancer; FOXF1; Intronic copy-number variants; Splicing;
机译:新型FOXF1深度内含子缺失导致致命的肺发育异常,肺泡毛细血管发育不良和肺静脉错位
机译:肺泡毛细血管发育不良,具有在FoxF1 FoxF1内框架缺失引起的肺静脉和软质左心序列的错位
机译:致命性肺泡毛细血管发育不良伴肺静脉错位的情况下FOXF1的倒位
机译:新型FOXF1深度内含子缺失导致致命的肺发育异常肺泡毛细血管发育不良肺静脉排列不全
机译:新型FoxF1深入内肠缺失导致致命肺部发育障碍,肺泡毛细血管发育不良,具有肺静脉未对准