1) nullizygoisty
缺合子性
2) Electron-deficient property
缺电子性
4) Heterozygote deficiency
杂合子缺乏
1.
Except for Ningde Population,heterozygote deficiency existed in 13 polymorphic loci from the other 8 populations of F.
应用聚丙烯酰胺凝胶电泳技术,研究了长毛明对虾(Fenneropenaeus penicillatus)9个野生群体杂合子缺乏及过量情况;测定了8个酶系统,共检测到15个酶位点和32个等位基因。
5) loss of heterozygosity
杂合性缺失
1.
Identification of some macrosatillite sites of chromosome 19 in primary gastric carcinoma with loss of heterozygosity;
19号染色体微卫星杂合性缺失与原发性胃癌的临床关系
2.
Analysis of loss of heterozygosity in tk gene of L5178Y mouse lymphoma cells induced by colchicine and vincristine;
秋水仙碱和长春新碱诱导L5178Y小鼠淋巴瘤细胞tk基因杂合性缺失分析
3.
Study of loss of heterozygosity and microsatellite instabilities of fragile histidine triad gene in gastric carcinoma;
胃癌FHIT基因杂合性缺失及微卫星不稳定性的研究
6) Homozygous deletion
纯合性缺失
1.
Detection of homozygous deletion and mutation of exon 5 and exon 8 of FHIT gene in differentiated thyroid carcinoma tissue;
分化型甲状腺癌组织中脆性组氨酸三联体基因外显子5、8纯合性缺失及突变检测
2.
The homozygous deletion was detectyed by multiple PCR analysis and mutation by PCR-SSCP and DNA sequencing followed.
方法采用多重PCR、PCR-SSCP和DNA测序对62例胃癌、癌旁组织及10例正常胃黏膜标本中p16INK4a基因纯合性缺失和突变进行检测。
3.
Aim: To investigate the frequencies of homozygous deletion of entire coding exons of fragile histidine triad (FHIT) gene in laryngeal squamous cell carcinoma (LSCC) tissue and its clinical significance.
目的:探讨喉鳞癌(LSCC)组织中脆性组氨酸三联体(FHIT)基因编码外显子纯合性缺失及其临床意义。
补充资料：缺铁性假膜性食管炎
缺铁性假膜性食管炎
参见"铁缺乏性吞咽困难"。
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