A case with 9q33.3 microdeletion pointing to the existence of a new syndrome unrelated to STXBP1 gene deletionDavit BabikyanEUROPEAN JOURNAL OF HUMAN GENETICS（2023）引用 0|浏览6AI 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
