Alagille Syndrome Due to a De Novo NOTCH2 Mutation Presenting As Prenatal Oligohydramnios and Congenital Bilateral Renal Hypodysplasia: A Case Report
Frontiers in Pediatrics（2022）
关键词
Alagille syndrome,NOTCH2 gene,prenatal oligohydramnios,congenitally bilateral renal hypodysplasia,case report
AI 理解论文
溯源树
样例
生成溯源树，研究论文发展脉络
Chat Paper
正在生成论文摘要