CATSHL SYNDROME: CONFIRMATORY MULTIGENERATIONAL FAMILY OF A UNIQUE AND RECOGNIZABLE PHENOTYPE DUE TO A CONSISTENT MUTATION IN FGFR3L. F. Escobar,M. Bamshad, M. E. Tucker, A. L. HallAMERICAN JOURNAL OF MEDICAL GENETICS PART A（2015）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
