15q26.3 deletions distal to IGF1R cause growth retardation, congenital heart defect and skeletal anomalies: Case report and review of literature

导出原文传递

翻译打印收藏纠错

作者： Theru A. Sivakumaran ^[1] ; Theresa A. Grebe ^[2]

作者单位： Division of Pathology and Laboratory Medicine,Phoenix Children's Hospital ^[1] Department of Child Health,University of Arizona College of Medicine‐Phoenix ^[2]

关键词 15q26.3 deletion congenital heart defect dysmorphic facial features eye anomalies growth retardation skeletal anomalies

发布时间 2023-10-10

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

2023年191A卷9期

2392-2397页

相似文献

中文期刊
外文期刊
学位论文
会议论文

检索历史清除

15q26.3 deletions distal to IGF1R cause growth retardation, congenital heart defect and skeletal anomalies: Case report and review of literature

American journal of medical genetics, Part A

相似文献

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

15q26.3 deletions distal to IGF1R cause growth retardation, congenital heart defect and skeletal anomalies: Case report and review of literature

American journal of medical genetics, Part A

相似文献

American journal of medical genetics, Part A

相关期刊

检索历史清除