Case report-1q44 microdeletion and two heterozygous variants of DOLK gene in a patient with multiple congenital anomalies
EUROPEAN JOURNAL OF HUMAN GENETICS(2023)
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
EUROPEAN JOURNAL OF HUMAN GENETICS(2023)