P333: Exome sequencing identifies likely pathogenic variants in NF1, LMNA, and SDHC in individual with learning disability and multiple congenital anomalies
Genetics in Medicine Open(2024)
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
Genetics in Medicine Open(2024)