| 1. | Detection of fetal rhd types with maternal plasma for prenatal diagnosis
定量分析在产前性别诊断中的应用 |
| 2. | ( 2 ) rh d genes of rh d - negative individuals with c antigens have polymorphism
带有c的rhd阴性个体基因结构具有多态性。 |
| 3. | Rhd right - hand side
右座驾驶 |
| 4. | Results : phenotype frequency of rh c and rh e in individuals with rh d negative were 25 % and 3 % respectively
结果：中国人rhd阴性个体中， c和e的表型频率分别为25和3 。 |
| 5. | ( 5 ) " normal " rh d exon # 4 amplifying product did not be found in all the samples , instead of 37bp insert
全部rhd阴性和阳性汉族和维族个体中都没有发现“ nomal ” rhdexon # 4 ，扩增产物都是37bp插入片段。 |
| 6. | The polymorphism of rh d gene structure of han nationality of chinese was significantly different from caucasian and wei nationality characteristic
中国汉族人群在rhd基因结构多态性上与高加索人种显著不同，而维族人群则另具特征。 |
| 7. | ( 2 ) gene structure of the rh d - negative in chinese have polymorphism , especially in the individuals with c antigen , which accorded with the oriental character . d gene exon of chinese polymorphism expressed for intact , partial deletion and total deletion , and probably existed specific d ( nf ) ce haplotype
中国人rhd基因结构具有多态性，特别是带有c的个体，符合东方人具有完全缺失、部分缺失和不缺失三种情况，并可能存在特殊的d ( nf ) ce单体型。 |
| 8. | The individuals of rhd - positive phenotype with intact exons carried generally insert fragments and boxl box2 and box3 and this proved that inserts or rh box could n ' t affect the express of rh d gene . in 2 of the 5 wei nationality pedigrees whose proband were rh d - negative , rhc / e phenotype of all the rh negative individuals was ccee . rhd exon 4nsert and rh box did not be found in all individuals
在7个先证者为rhd阴性的汉族家系中，大部分成员均出现插入片段和rhbox ，且在遗传上符合孟德尔遗传定律， d外显子完整且表型为rhd阳性的家系个体成员广泛带有插入片段和box1 、 box2或box3 ，插入片段或rhbox并未影响d基因的表达。 |
| 9. | In 82 cases of rh d serology negative individuals with rh c / e typing for cc or cc was 20 , of which 9 carried intact exons , 6 carried partial deletion exons , and 5 was total deletion . ( 3 ) inseit fragments and rh box were detected in most of cases in 7 han nationality pedigrees which proband were rh d - negative , and intheritance accorded with the mendel ' s law
检测82例rhd血清学阴性个体中， c e型为cc或cc有20例，其中完整携带rhd基因外显子者为9例，部分携带者为6例，完全缺失者为5例。 |
| 10. | To study on structure and inheritance of rh d gene interaction between gene expression of rh d and rh c / e and influences on rh d gene expression of inserts and rh box - methods : 20 pairs of oligonucleotide specific primers for exon , intron 2 4 , insert and rh box of rh d , rhc / e gene were designed and composed the polymerase chain reaction - sequence specific oligonucleotide primer ( pcr - ssp ) was used to amplify the rh c / e gene , rh d gene , exon , intron , insert and rh box in 106 samples of unrelated individuals and 7 han nationality ancestries and 5 wei nationality ancestries whose proband were rh d - negative
目的：观察中国汉族非血缘关系随机个体、汉族及维吾尔族家系rh血型的c e基因、 d基因外显子、内含子、插入片段以及rhbox ，研究rhd基因结构及遗传规律， d基因表达与c e基因的关联，以及插入片段和rhbox对d基因表达的影响。 |
