机译:TFAP2B TFAP2B中的一种新型致畸突变与CHAR综合征和中央糖尿病患者
Division of Newborn MedicineDepartment of Pediatrics Boston Children's Hospital and Harvard;
Division of Genetics and GenomicsDepartment of Pediatrics Boston Children's Hospital and Harvard;
Division of Newborn MedicineDepartment of Pediatrics Boston Children's Hospital and Harvard;
Division of Genetics and GenomicsDepartment of Pediatrics Boston Children's Hospital and Harvard;
Department of Otolaryngology and Communication EnhancementBoston Children's Hospital and Harvard;
Division of Newborn MedicineDepartment of Pediatrics Boston Children's Hospital and Harvard;
Division of EndocrinologyDepartment of Pediatrics Boston Children's Hospital and Harvard Medical;
Division of Newborn MedicineDepartment of Pediatrics Boston Children's Hospital and Harvard;
Char syndrome; diabetes insipidus; patent ductus arteriosus; TFAP2B protein; human; transcription factor AP‐2;
机译:TFAP2B TFAP2B中的一种新型致畸突变与CHAR综合征和中央糖尿病患者
机译:一种涉及TFAP2B基因的家族性Char综合征,重点是面部形状特征
机译:动脉导管未闭综合征:单倍型TFAP2B突变不足的证据和连锁睡眠障碍的鉴定
机译:合并抑郁症和糖尿病药物治疗的挑战
机译:中枢尿崩症患者血浆渗透压的闭环控制
机译:导致字符综合征的新型TFAP2B突变提供了基因型-表型的相关性。
机译:导致字符综合征的新型TFAP2B突变提供了基因型-表型的相关性。