Expanding the phenotype of cerebellar-facial-dental syndrome: two siblings with novel homozygous mutation in BRF1M. Codina,I. Valenzuela,I. Paramonov, M. Benjumea,S. Siso,E. Garcia-Arumi,E. Tizzano,I. CuscoEUROPEAN JOURNAL OF HUMAN GENETICS(2019)引用 4|浏览18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