Variant in HNRNPR leading to developmental delay with facial dysmorphism and bone abnormalities: a case reportMarie Massier,Marta Spodenkiewicz,Nathalie Bednarek,Boris Keren,Emilie Landais, Lucas Herissant,Celine Poirsier-Violle,Martine Doco-FenzyEUROPEAN JOURNAL OF HUMAN GENETICS(2022)引用 0|浏览10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