The diagnosis of the first-documented intragenic KANSL1 microduplication patient broadens the genetic spectrum of Koolen de Vries syndromeLoreto Martorell,Delia Yubero,Esther Cuatrecasas Capdevila,Guerau Fernandez Isern, Diana Salinas, Rosanna Mari Vico,Monica Rebollo,Jordi Muchart,Judith Armstrong,Juan Dario Ortigoza-EscobarClinical Genetics(2022)引用 0|浏览9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