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imperfecta
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  “imperfecta”译为未确定词的双语例句
     Mutation Detection of COL1A1 Gene in a Pedigree with Osteogenesis Imperfecta
     一成骨不全家系的COL1A1基因突变检测
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     Methods The blood samples were collected from the family with dentinogenesis imperfecta type Ⅱ including 18 individuals. We perform genetic linkage analyse of 6 short tandem repeat loci at the region of 4q21(D4S1534、GATA62A11、DSP(P)、DMP1、SPP1、D4S1563)as well as haplotyping by fluorescent- PCR.
     方法提取在南京地区发现的一个牙本质生长不全Ⅱ型家系18成员的外周血DNA,在染色体4q21上选择6个短串联重复序列(short tandem repeat,STR)位点,即D4S1534、GATA62A11、DSP(P)、DMP1、SPP1和D4S1563用连锁分析法分析该家系疾病基因与上述6个STR位点的连锁关系并进行染色体单倍型分型。
     Over 90% of patients with osteogenesis imperfecta have mutations in the COL1A1 and COL1A2 genes which encode the chains of typeⅠprocollagen.
     90%以上病例的发生与形成Ⅰ型胶原的两个基因(COL1A1和COL1A2)突变有关。
短句来源
     X-ray Diagnosis of Osteogenesis Imperfecta:A Report of 10 Cases and Literature Review
     成骨不全症的X线诊断(附10例报告及文献复习)
短句来源
     Materials and Methods: The clinical manifestations and X-ray features of 21 cases (fetus 1 case, new-born baby 6 cases, infant 4 cases, children 6 cases, adult 4 cases) of osteogenesis imperfecta were reported and analysed.
     资料与方法:报告21例(胎儿1例,新生儿6例,婴儿4例,儿童6例,成人4例)成骨不全的临床及X线平片观察。
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  相似匹配句对
     The diagnosis of osteogenesis imperfecta
     成骨不全的X线诊断
短句来源
     Familial Osteogenesis Imperfecta
     家族性成骨不全
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  imperfecta
Microhardness and microstructure of deciduous enamel with different types of amelogenesis imperfecta
      
Amelogenesis imperfecta (AI) is an inherited tooth disorder with widely varying phenotypes.
      
Surgical treatment of the femur in osteogenesis imperfecta with intramedullary elongating rods
      
Beitrag zur Lehre von der Osteogenesis imperfecta tarda
      
Amelogenesis imperfecta-kieferorthop?dische Probleme und deren L?sung mit Hilfe von Multibandapparaturen und tempor?ren Stahlkro
      
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Pedigrees of two osteogenesis imperfecta Hui-probands were reported and analyzed, suggested an autosomal dominant inheritance in one family with eleven affected patients in three successive generations of 23 family members, an autosomal recessive in the other family without any affee ted relatives in four successive generations except the femalechild prod and herself. The latter family, sthird f ilia 1 consists of onlytwo children, of which a seven-year old girl Ⅳ_1 is the sibling sister of proband Ⅳ_2;...

Pedigrees of two osteogenesis imperfecta Hui-probands were reported and analyzed, suggested an autosomal dominant inheritance in one family with eleven affected patients in three successive generations of 23 family members, an autosomal recessive in the other family without any affee ted relatives in four successive generations except the femalechild prod and herself. The latter family, sthird f ilia 1 consists of onlytwo children, of which a seven-year old girl Ⅳ_1 is the sibling sister of proband Ⅳ_2; the proband's parents are of (?)onsanguineous marriage whose mothers are sisters of sibling relation.

报告二个成骨不全症回族家系。家系调查和系谱分析表明,一个家系连续三代都有发病的,26人中共有11人罹患本症,为常染色体显性遗传;另一个家系先证者的父母为姨表兄妹近亲联姻,家系中连续4代(包括先证者的7岁姐姐在内)无一人见有本症,考虑为常染色体隐性遗传。

Pedigrees of two osteogenesis imperfecta Hui-proands were reported and analyzed, suggesting an autosomal dominant inheritance in one family and an autosomal recessive in the other. In the eleven surviving child and adult patients including the two probands, all having blue sclerae and deformities resulting from fracture and repeated fractures, chromosomes preparations of peripheral blood lymphocytes culture specimens stained by the Gbanding technique were karyotyped; serum Ca, P, T_4, T_3 and corticosteroids...

Pedigrees of two osteogenesis imperfecta Hui-proands were reported and analyzed, suggesting an autosomal dominant inheritance in one family and an autosomal recessive in the other. In the eleven surviving child and adult patients including the two probands, all having blue sclerae and deformities resulting from fracture and repeated fractures, chromosomes preparations of peripheral blood lymphocytes culture specimens stained by the Gbanding technique were karyotyped; serum Ca, P, T_4, T_3 and corticosteroids as well as blood AKP, urine 17-OHCS and 17-KS assaying and examinations were performed, the endocrinological mechanisms in the pathogenesis of this anomaly were briefly discussed together with the biochemical metabolic changes

报道了两例回族成骨不全先证者各各的常染色体显性遗传和常染色体隐性遗传家系。结合两家系中的11例患者,进行了临床激素检测,钙、磷生化检验和染色体核型分析等方面的内分泌和代谢的病因学探讨。

Surveys of fungal diseases of 16 species of cultivated grass and 10species of Legume were made in 10ess Plateau of Eastern Gansu Province during 1983 and 1985.Of 43 diseases found on legumes,the common ones are Uromyces rusts,Stemphylium leaf spot(S.botryosum and s.sarciniformii)Ascochyta black stem (A.imperfecta)Ascochyta stem canker—like disease(A.sp.)and Fusarium root rot(Fusarium spp.).Fifty diseases were identified.on grasses.Most frequently found ones are crown rust(Puccinia coronata),stem rust(P.graminis),leaf...

Surveys of fungal diseases of 16 species of cultivated grass and 10species of Legume were made in 10ess Plateau of Eastern Gansu Province during 1983 and 1985.Of 43 diseases found on legumes,the common ones are Uromyces rusts,Stemphylium leaf spot(S.botryosum and s.sarciniformii)Ascochyta black stem (A.imperfecta)Ascochyta stem canker—like disease(A.sp.)and Fusarium root rot(Fusarium spp.).Fifty diseases were identified.on grasses.Most frequently found ones are crown rust(Puccinia coronata),stem rust(P.graminis),leaf rust(P.recondita),stripe rust(P.striiformis),Ascochyta leaf spot(A.sorghi),Bipolaris leaf spot (B.sorokiniana)and Tar spot(Phyllachora graminis).The disease resistance of each host and the possible ways for disease control in this enviroment were descussed.

1983年和1985年,对陇东黄土高原栽培豆科和禾本科牧草的真菌病害,进行了采集和调查,分离和鉴定出真菌44种。在10种豆科牧草上,共发现了43种寄主一病原真菌组合。其中最常见者为锈病,匍柄霉叶斑病,壳二孢黑茎病,壳二孢类茎溃疡病,和镰刀菌根腐病。在16种禾本科牧草上,共发现50种寄主—病原真菌组合。其中以各种锈病,壳二孢叶斑病,二极孢叶斑病,和黑痣病等发生最为普遍。对牧草的抗病性给予了初步评价。就当地条件下病害治理提出了建议。

 
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