P272: Uniparental disomy of chromosome 19 in an individual with oculocutaneous albinism, neurodevelopmental disorder, and failure to thrive
Genetics in Medicine Open（2023）
关键词
neurodevelopmental disorder,chromosome,uniparental disomy,oculocutaneous albinism
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