A case of familial brain-lung-thyroid syndrome due to a NKX2.1 run-on mutationFederica Baldan,Elena Cavaliere,Anna J. Gortan,Nadia Passon,Dora Fabbro,Dario Marin,Myriam Carecchio,Sara C. Credendino,Rosa Gallo,Paola Cogo,Giuseppe Damante,Gabriella De VitaEUROPEAN JOURNAL OF HUMAN GENETICS(2022)引用 0|浏览8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