1) terminal deletion
末端缺失
1.
Objective To determine the karyotype of a case with a history of spontaneous abortion and terminal deletion by using of conventional G banding method and search the cause of insertional translocation of chromosomal terminal region.
目的 确定一个有反复流产史且常规 G显带发现有 7q末端缺失病例的核型 ,探讨染色体末端区域插入易位的形成机理。
2) N terminal deletion
N末端缺失
3) N-terminal deletion
N-末端缺失
4) C-terminal deleted mutant
羧基末端缺失
1.
AIM: To construct a recombinant eukaryotic expression vector encoding C-terminal deleted mutant of hepatitis C virus (HCV) core protein and express it in P815 cell line.
目的:构建羧基末端缺失核蛋白的真核表达载体并在小鼠肥大细胞瘤细胞株P815细胞中表达。
5) free-end edentulous
末端游离缺失
1.
Methods Models for bilateral mandibular free-end edentulous (765 567) and parametric prosthetic models were combined to establish the three-dimensional finite element model libraries by means of HyperMesh 7.
目的建立下颌双侧末端游离缺失修复方案的有限元模型库。
6) C-terminal truncated analog
C末端缺失变异体
补充资料：21号染色体部分缺失综合征
21号染色体部分缺失综合征
病名。即21q-综合征。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条