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
Department of Obstetrics and Gynecology The Prenatal Diagnosis and Medical Genetics ProgramMount;
Division of Clinical and Metabolic Genetics Department of PediatricsThe Hospital for Sick Children;
Department of Obstetrics and Gynecology The Prenatal Diagnosis and Medical Genetics ProgramMount;
Department of Obstetrics and Gynecology The Prenatal Diagnosis and Medical Genetics ProgramMount;
Department of Paediatric Laboratory Medicine Genome Diagnostics Laboratory Medicine and;
Division of Clinical and Metabolic Genetics Department of PediatricsThe Hospital for Sick Children;
Department of Paediatric Laboratory Medicine Laboratory Medicine and PathobiologyThe Hospital for;
Department of Obstetrics and Gynecology The Prenatal Diagnosis and Medical Genetics ProgramMount;
alveolar capillary dysplasia; Forkhead transcription factors; Hypoplastic left heart syndrome; intestinal atresia;
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: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: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
机译:左侧壁壁和食道之间解剖关系的CT扫描评估,以及肺静脉隔离后后果后果
机译:两个缺失与遥远的FOXF1增强子重叠揭示了lncRNA LINC01081在肺静脉毛排列不齐的肺泡毛细血管发育不良的病因中的作用
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