heterozygote
heterozygote
1. 1 patient of 129 Met/Val heterozygote showed abnormal signals in basal ganglia after 12 months, and survived for 16 months.
1例甲硫氨酸杂合型 (12 9Met/Val)底节异常信号发现时间为 12个月 ,存活时间为 16个月 ;
2. The mutant result LSD-t check of the 2 sites showed that mean difference of homozygote and heterozygote, homozygote and concentration of wild type homocysteine had statistical significance (P < 0.05).
2个位点突变结果LSD-t检验显示纯合子与杂合子,纯合子与野生型血浆同型半胱氨酸浓度均数差有统计学意义(P<0.05)。
3. In children the frequency of heterozygote was 35.7% and allele(+) was 17.9%,that similar to internal reports(14.7%),but much less than caucasian(43%).
30 8名儿童杂和突变型检出率为 35 7% ,等位基因 (+)频率为 17 9% ,与国内其它报道相近 (14 7% ) ,但远低于白种人群频率 4 3% ;
4. The patients’ with 5G homozygotes had the lowest levels of plasma PAI-1.The patients’ with heterozygote were intermediate. 3.
5G纯合子的血浆PAI-1抗原水平最低，4G/5G杂合子者其抗原水平居于两者之间。
5. Conclusions: SSR could effectively distinguish heterozygote from homozygote, which makes it an ideal tool for the authentication of wild and cultivated Gastrodia elata Bl. at molecular level.
SSR分子标记可有效地区分纯合子及杂合子，从而使其能够在分子水平鉴定野生和栽培天麻。
6. STR could identify homozygote and heterozygote of mouse; 28 of 40 STR loci were polymorphic among morse strins, and 8 lsci were significantly polymorphic;
STR可识别动物品系的纯合子与杂合子,40个STR位点中28个位点具有品系间多态性,8个位点具有显著多态性;
7. Microsatellite TNFc polymorphism had two alleles (TNFc1 and TNFc2) and three kinds of genotype (homozygotes TNFc1c1 and TNFc2c2, and heterozygote TNFc1c2). The genotype distribution fit Hardy Weinberg equilibrium.
TNFc微卫星多态性含有 2个等位基因 (TNFc1和TNFc2 )及 3种基因型 (纯合子 1/ 1、2 / 2及杂合子 1/ 2 ) ,基因型分布符合Hardy Weinberg平衡定律。
8. A Report of Three Cases of Abnormal Hemoglobins and Double Heterozygote HbQ+H
三例异常血红蛋白与HbQ+H双重杂合子研究
9. Heterozygote deficiency coefficients (F) of the two populations in Daya Bay and Beibu Gulf were -0.278 and -0.346,respectively;
两个种群的杂合子缺失系数分别为-0.278和-0.346;
10. The cross between sub-acid varietties of heterozygote can increas the ratio of selective preponderance in progenies.
主基因显性纯合的中酸品种相互间或与杂合品种间交配可增加后代群体优选率,提高育种效果。
11. The results of LSD-t test of the mutation at the two sites showed that there were significant differences between homozygote and heterozygote, homozygote and wild type, as well as C heterozygote and wild type (P < 0.05).
二个位点突变结果LSD-t检验显示:纯合子与杂合子,纯合子与野生型,C杂合子与野生型间差异均有显著性意义(P<0.05)。
12. inversion heterozygote
倒位杂合子
13. A condition in which both alleles of a gene pair in a heterozygote are fully expressed, with neither one being dominant or recessive to the other.
共显性在异型结合体中一个基因对的两个等位基因完全传递的条件，两者相对无优劣之分
14. A condition in which both alleles of a gene pair in a heterozygote are fully expressed,with neither one being dominant or recessive to the other.
共显性在异型结合体中一个基因对的两个等位基因完全传递的条件，两者相对无优劣之分。
15. Of or relating to two alleles of a gene pair in a heterozygote that are both fully expressed.
共显性的属于或有关异型结合体中一个基因对的两个等位基因都已完全传递的
16. Keywords Muscular atrophy;spinal;Gene;SMN;Multiplex ligation-dependent probe amplification;Gene deletion;Heterozygote detection;
关键词肌萎缩;脊髓性;基因;SMN;多重连接探针扩增法;基因缺失;杂合子检测;
17. Haploid embryos which only with chromosome of female parent were obtained due to the chromosome elimination of pollen parent quickly and completely during the heterozygote development.
利用杂合子发育过程中来自父本的染色体完全、迅速地消失得到大量单倍体胚。
18. enforced heterozygote
加强异质结合体
19. double heterozygote
双杂合体
20. Comparing to contrals, there was a trend toward an increased frequency of the G/G and A/A homozygote, but a trend toward a decreased frequency of the G/A heterozygote in the PD cases.
和对照组比较，PD组野生型和突变型纯合子（G/G和A/A）的频率分布有增高趋势，而杂合子基因型（G/A）的分布则有降低趋势。
21. Unimodal distribution of TPMT activity was found in Chinese Kazakstan. Only TPMT*3C and TPMT*3A heterozygote was found in Kazakstan Chinese.
哈萨克族T PMT活性呈正态分布,活性的均值为(12.27±3.42)U·mL-1 Rbc,其中发现6 例TPMT*3C杂合子和2例TPMT*3A杂合子,总TPMT基因突变频率是1.2%。
22. We conclude that PFIC heterozygote status of the donor does not increase the risk of liver dysfunction in either recipients or donors, with a similar course compared with BA recipients and donors.
因此我们得出以下结论，即PFIC杂合子并不会增加受体和捐赠者术后肝脏失功能的风险；BA受体和捐赠者也出现相似的结果。
23. Keywords Thalassemia;Gene;Heterozygote;Polymerase chain reaction;Reverse dot blot;
地中海贫血;基因;杂合子;聚合酶链反应;反向点杂交;
24. complex heterozygote
复合杂合子
25. Keywords p53 codon 72;polymorphism;homozygote;heterozygote;HPV-associated cervical cancer;
多态性;纯合子;杂合子;HPV有关的宫颈癌;
26. a person with a pair of di imilar alleles is a heterozygote.
如带有两个不相同的等位基因,则为杂合子.
27. For XRCC2 C41657T, both heterozygote and homozygote T carriers have the increased risk of developing adenosquamous carcinoma, the heterozygote CT carriers have the increased risk of developing lung cancer in non smokers.
对于XRCC2C41657T多态位点,携带T等位基因的基因型可能增加腺鳞癌的发病风险,C/T基因型可能增加不吸烟者患肺癌风险;
28. of or relating to two alleles of a gene pair in a heterozygote that are both fully expressed
属于或有关异型结合体中一个基因对的两个等位基因都已完全传递的
29. balanced double heterozygote
平衡二重杂合体, 平衡二重杂合子, 平衡二重异型接合体, 平衡二重异型接合子
30. diploid heterozygote
异质二倍体, 二倍体异质接合子
31. heterozygote A diploid organism or cell that has inherited different alleles, at a particular locus, from each parent.
异质接合体已经遗传不同等位基因的一个双倍体生物或细胞，在一个特定的位点，分别从父母双方。
32. sex heterozygote
性杂合体; 性别杂种
33. Under the conditions of random mating and selecting.The research by compute r simulation analysed the possibility of long-time conserving heterozygote in co long.
摘要 本文运用计算机模拟的方法，在随机交配、随机留种的情况下，分析了群体中长期保存 杂合子的可能性。
34. A compound heterozygote family of familial hypercholesterolemia due to new mutations
新突变致复合杂合子家族性高胆固醇血症家系的基因检测
35. tranlocation heterozygote
易位异型接合体
36. manifesting heterozygote
显性杂合子
37. Finally, the homozygote generation is obtained by self-cross mating of the second heterozygote.
最后,第二代杂合体自交可以获得纯合体。
38. heterozygote superiority
杂合优势, 异型优势
39. An allele that, in a heterozygote, prevents the expression of another (recessive) allele at the same locus.
杂合体生物与显性纯合体生物具有相同的表现型。
40. Of or relating to a heterozygote.
杂合体的杂合体的或与之有关的
41. heterozygote advantage
杂合子优势
42. heterozygote detection
杂合子检出
43. heterozygote proportion
杂合子比例
44. gene with the heterozygote
杂合子的单基因
45. heterozygote screening
杂合子筛查
46. Heterozygote deficiency
杂合子缺乏
47. Contrast this fact with the very different outcome of crossbreeding between two genetically distant members of the same species where the result is often heterozygote advantage (hybrid vigor).
正是同种远基因成员间的杂交产生不同的结果，而产生杂种优势。
48. permanent heterozygote
永久杂合体
49. In this paper we have used the double heterozygote as female parent and the good line as male parent in cross and backcross.
然而，以双杂合体为母本，优良自交系为父本，二者杂交或进行回交，再在杂种后代中选准双杂合体做母本，继续进行自交或回交，是较快而有效的方法。
50. The heterozygote Y/y may be distinguished by the nectary color
用蜜腺颜色就可以确定为异质结合的(Y;y)。
51. The heterozygote Y/y may be distinguished by the nectary color.
用蜜腺颜色就可以确定为异质结合的（y/y）。
52. 3. The heterozygote Y / y may be distinguished by the nectary color.
用蜜腺颜色就可以确定为异质结合的（y／y）。
53. Owing to the influence of various complex factors,it is possible for the heterozygote of autosomal dominant inheritance to appear in different phenotypes.
由于各种复杂因素的影响,常染色体显性遗传的杂合子有可能出现不同的表现型,本文阐述了常染色体显性遗传的几种类型。
54. repulsive heterozygote
相斥杂合子
55. structural heterozygote
结构杂合子
56. The incidence of C3 deficient heterozygote was 15.7%.
结果发现具有第三补体缺损的异型合子在这个族群的发生率为15.7%。
57. Results For the same SNP locus, the homozygote showed a single product peak, and the heterozygote showed two product peaks with different length.
结果每个SNP纯合子为单一产物峰，杂合子则为长度不同的两个产物峰。
58. The reasons for the production of heterozygote and homozygote in Gastrodia elata Bl. were self-breeding and cross-breeding respectively.
结论：天麻的自交及杂交是形成纯合与杂合的原因。
59. deletion heterozygote
缺失杂合体[子] 缺失异型接合子[体]
60. deficiency heterozygote
缺失杂合子
61. Keywords Liver neoplasms;Chromosomes;Heterozygote;Genes;
肝肿瘤;染色体;杂合子;基因;
62. cytoplasmic heterozygote
胞质杂合子
63. Keywords Hemophilia A;Heterozygote detection;Polymerase chain reaction;
血友病A;杂合子检测;聚合酶链反应;
64. Keywords corneal dystrophy;TGFBI gene;autosomal dominant inheritance;heterozygote;mutations;
角膜营养不良;TGFBI基因;常染色体显性遗传;杂合子;突变;
65. the condition of a heterozygote having a phenotype that is more pronounced or better adapted than that of either homozygote
超显性杂合了具有产生比纯合子延伸更长或适应性更好的表现型的条件
66. Of them, 11 markers deviated to wards pollen parent Shennong 606 and 12 markers towards ovule parent Lijiangxintuanheigu, only one towards heterozygote.
这些偏分离位点中偏向沈农606基因型的有11个；偏向丽江新团黑谷基因型的有12个；仅有1个偏杂合体类型。
67. partial heterozygote
部分异质接合子
68. recombinational heterozygote
重组的异质结合体
69. cis heterozygote
顺式杂合子, 顺式杂合体
