A Japanese familial case of hypochondroplasia with a novel mutation in <i>FGFR3</i>Keiko Nagahara,Yuki Harada,Tohru Futami,Masaki Takagi,Gen Nishimura,Yukihiro HasegawaClinical Pediatric Endocrinology(2016)引用 0|浏览2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