A De Novo Missense Mutation Highlights The Role Of Fbxo28 Gene In 1q41-Q42 Microdeletion Syndrome PhenotypeN. Spataro,E. Gabau, N. Baena,M. Guitart,A. RuizEUROPEAN JOURNAL OF HUMAN GENETICS（2020）引用 0|浏览3暂无评分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
