首页> American journal of medical genetics, Part A> Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3' terminus of the FBN1-gene.

Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3' terminus of the FBN1-gene.

导出原文传递

翻译打印收藏纠错

第一作者： Graul Neumann LM

作者： Graul Neumann LM ^[1] ; Kienitz T ; Robinson PN ; Baasanjav S ; Karow B ; Gillessen Kaesbach G ; Fahsold R ; Schmidt H ; Hoffmann K ; Passarge E

作者单位： Institut fur Humangenetik, Charite Universitatsmedizin Berlin, Berlin, Germany. ^[1]

发布时间 2013-11-20

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交

浏览0

American journal of medical genetics, Part A

2010年152A卷11期

2749-2755页

相似文献

中文期刊
外文期刊
学位论文
会议论文

浏览0

American journal of medical genetics, Part A

2010年152A卷11期

2749-2755页

检索历史清除

Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3' terminus of the FBN1-gene.

American journal of medical genetics, Part A

相似文献

同项目论文

American journal of medical genetics, Part A

相关期刊

参考文献：
指定格式：	NoteExpress EndNote RefWorks NoteFirst

检索历史 清除

Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3' terminus of the FBN1-gene.

American journal of medical genetics, Part A

相似文献

同项目论文

American journal of medical genetics, Part A

相关期刊

检索历史清除