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患者双亲
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  patients ' parents
     The most commontype of HBVM infection was the positive of HBsAg,anti-HBe and anti-HBC simultaneously,which was in accordance with HBVM type in PHC patients attacked by HBV.2. In the fullbrothers and sisters of PHC patients,the positive rate of HBVM was 82. 98% and HBsAg,51. 0% which were obviously higher than those the patients' parents and children (P <0. 05 ).
     其HBVM最常见模式是HBsAg、抗-HBe和抗-HBc同时阳性,与有HBV感染的PHC患者HBVM的最常见模式相一致。 2.患者同胞的HBVM阳性率为82,98%,HBsAg为51.0%,均显著高于患者双亲、子代(P<0.05);
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  “患者双亲”译为未确定词的双语例句
     Chromosome aberration and micronucleuswere determined by mitomycin C (MMC) 、acetic aldehyde (AA) or ethanol (EtOH) inducing in 36 cases of Klinefelter syndrome, their 56 parents and 45 controls.
     为了解诱变剂对Klinefelter综合征发生的影响,对Klinefelter综合征患者、患者双亲及对照进行丝裂霉素C、乙醛或乙醇诱导非二倍体、染色体结构畸变及微核观察,发现丝裂霉素C诱导的患者染色体结构畸变和微核均显著多于对照和双亲。
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     Objectives In order to explore the cytogenetic mechanism of aneuploid occurrence,this paper investigated the variations of centromeric dots(Cd),the activity alteration of nucleolar organizer region(NOR)rRNA genes and the frequencies of Ag-AA of aneuploid patients and some of their parents.
     目的 研究非整倍体患者及部分患者双亲染色体着丝粒点 (Cd)结构变异、核仁组织区 (NOR)rRNA基因活性变化和银染近端着丝粒染色体联合 (Ag -AA )频率 ,探讨非整倍体畸变的细胞遗传学机理。
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     No mutation was found in the family members including the parents of the proband. So, Argl70Gln was considered as the de novo mutation.
     对突变携带者进行家系调查,患者双亲及其他家系成员未携带该突变,故该突变为de novo突变。
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     On the other hand, the examination of their parents revealed no abnormality.
     而患者双亲则与本实验室正常组对照无特殊异常。
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     To further illustrate the biological significance of variant NOR (including double NOR-dNOR and triple NOR-tNOR) and satellite association (SA) and the relationship to meiotic 'non-disjunction (NDJ),this study was carried out in the normal population and the parents of patients with Down Syndrome (DS).
     本文以硝酸银染色法研究了200对正常夫妇及200对唐氏综合征(DS)患者双亲淋巴细胞染色体核仁形成区(NOR)。
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  相似匹配句对
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     视网膜母细胞瘤患者双亲染色体不稳定性观察
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     The Chromosome Karyotype Analysis on 155 Cases myasthenia of Patients and Their Parents
     155例肌无力患者及其双亲染色体核型分析
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     P were analyzed retrospectively.
     P患者的资料。
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     The Circulating Immune Complexes in Patients with Uveitis
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  patients ' parents
One patients' parents refused surgery for the CLH after treatment of a hydrometrocolpos and another died of fulminant pneumonia before the operation.
      
Evaluation included subjective findings, especially the views of the patients' parents, and objective findings, including chest radiographs, computed tomography (CT), spirogram, electrocardiography, and echocardiography.
      
Follow up was carried out by personal interviews and interviews over the telephone with patients/parents.
      
The patients' parents were consanguineous, such that the patients were true homozygotes for the mutated GPI genes.
      
The manner of dealing with patients/parents, of winning their confidence, the art of listening to them, the art of soothing and consoling them-all this cannot be learnt from books.
      
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This paper presents the results of a study of chromosome analysis and sate-llite association of a female patient with G/G translocation Down's syndrome andpedigree.The patient has suffered from the G/G translocation Down's syndrome.The result can be concluded that the karyotypes of the patient's parents arenormal,then the abnormal chromosomes of the patient do not originate directlyfrom one of her parents.Perhaps,under the influence of some factors and duringthe course of meiosis,the chromosomes 21 of one of...

This paper presents the results of a study of chromosome analysis and sate-llite association of a female patient with G/G translocation Down's syndrome andpedigree.The patient has suffered from the G/G translocation Down's syndrome.The result can be concluded that the karyotypes of the patient's parents arenormal,then the abnormal chromosomes of the patient do not originate directlyfrom one of her parents.Perhaps,under the influence of some factors and duringthe course of meiosis,the chromosomes 21 of one of her parents give rise to non-disjunction.At the same time,between the homologous chromosomes 21,theyproduce new Robertsonian translocation.According to the frequency of the satellite association of the patient's parentsand other members in her pedigree,the numerical value is obviously higher thanthat of the contrast group,which provides an evidence for some scholars,thatis,the frequency of parents of a patient who suffers from Down's syndrome ishigher than that of the normal one.

本文报道了一个G/G易位型Down氏综合征患者的家系染色体分析和随体联合研究的情况.结果表明患者的双亲核型正常,患者异常染色体的来源可能是双亲之一的生殖细胞在减数分裂过程中,由于某些因素的影响,21号染色体发生了不分离,并且产生了21号同源染色体之间新的罗伯逊易位.统计患者双亲及其兄弟的随体联合频率,发现显著高于对照组正常人.为国外某些学者认为Down氏综合征患者双亲的随体联合频率高于一般人.提供了一个例证.

The results of the lymphocytic cultural studies of the whole peripheral blood from 3 patients with cerebral dysplasia showed that there were 3~5% of endoreduplication occurring in the phase of cell division. It should be considered as a high frequency endoreduplication. On the other hand, the examination of their parents revealed no abnormality. This phenomenon indicated that the high frequency of endoreduplication was not inherited by their parents. Therefore, we suggested that this high frequency of endoredupiication...

The results of the lymphocytic cultural studies of the whole peripheral blood from 3 patients with cerebral dysplasia showed that there were 3~5% of endoreduplication occurring in the phase of cell division. It should be considered as a high frequency endoreduplication. On the other hand, the examination of their parents revealed no abnormality. This phenomenon indicated that the high frequency of endoreduplication was not inherited by their parents. Therefore, we suggested that this high frequency of endoredupiication might be considered as one of the indexes of chromosome aberation of patients with serious mental retardation.

本文对3例重度智能障碍的男性患者以及其中2例的双亲,做了外周血淋巴细胞TC—199培养。染色体检查表明患者均有3~5%的内复制,是属罕见。而患者双亲则与本实验室正常组对照无特殊异常。初步认为内复制频率升高不受亲子代间传递的影响,可能与重度智能低下有相关性。

To further illustrate the biological significance of variant NOR (including double NOR-dNOR and triple NOR-tNOR) and satellite association (SA) and the relationship to meiotic 'non-disjunction (NDJ),this study was carried out in the normal population and the parents of patients with Down Syndrome (DS).Of 800 individuals,4 dNOR carriers,two of them from the control and two from the non-informative experiments were detected.SA data for 3 out of the 4 dNOR carriers showed no statistical significant increase in...

To further illustrate the biological significance of variant NOR (including double NOR-dNOR and triple NOR-tNOR) and satellite association (SA) and the relationship to meiotic 'non-disjunction (NDJ),this study was carried out in the normal population and the parents of patients with Down Syndrome (DS).Of 800 individuals,4 dNOR carriers,two of them from the control and two from the non-informative experiments were detected.SA data for 3 out of the 4 dNOR carriers showed no statistical significant increase in SA when dNOR was present in the cell even in case 4 where two dNOR were found in one cell.However,ease 3 demonstrated significant decraese in SA when dNOR was present,although it showed that the overall incidence of dNOR was higher in this carrier than that in the other three.It is concluded that dNOR can be detected on any acrocentric chromosome and not be related to NDJ of chromosome,which is a heritable variant that does not affect phenotype and that there are two kinds of dNOR variants,one being from the translocation of the short arm of acrocentric chromosome,the other from non-translocation.

本文以硝酸银染色法研究了200对正常夫妇及200对唐氏综合征(DS)患者双亲淋巴细胞染色体核仁形成区(NOR)。结果发现双核仁形成区(dNOR)的检出率在两组人群中均为0.5%;随体联合(SA)的结果表明,负有dNOR染色体的SA频率并不随其核糖体RNA(rRNA)基因含量的明显增加而上升,提示除rRNA基因含量及其活性外,尚有其他因素影响SA的形成。dNOR携带者与DS的发生亦无明显关系。

 
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