助手标题  
全文文献 工具书 数字 学术定义 翻译助手 学术趋势 更多
查询帮助
意见反馈
   osteogenesis imperfecta 的翻译结果: 查询用时:0.166秒
图标索引 在分类学科中查询
所有学科
外科学
特种医学
临床医学
生物学
妇产科学
儿科学
更多类别查询

图标索引 历史查询
 

osteogenesis imperfecta
相关语句
  成骨不全
     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
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。
短句来源
     X-ray examination and family-line investigation in 32 cases of osteogenesis imperfecta
     32例成骨不全症X线检查及家系调察分析
短句来源
     Objective To study the gene mutation of collagen, type Ⅰ, alpha 1(COL1A1) associated with the clinical characterization of a Chinese family with type I osteogenesis imperfecta (OI).
     目的探讨一个成骨不全家系的COL1A1基因的突变位点及其与临床特征的关系。
短句来源
更多       
  成骨不全症
     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
     X-ray examination and family-line investigation in 32 cases of osteogenesis imperfecta
     32例成骨不全症X线检查及家系调察分析
短句来源
     Methods The clinical and radiological manifestations of osteogenesis imperfecta in 10 child-patients were studied retrospectively.
     方法回顾性分析10例成骨不全症患儿的临床和X线表现。
短句来源
     Objective To discuss the X-ray appearances of osteogenesis imperfecta.
     目的探讨成骨不全症的X线诊断。
短句来源
     Conclusion Radiological manifestations have certain clinical value in the diagnosis and typing of osteogenesis imperfecta.
     结论X线表现对成骨不全症的诊断和分型有重要临床价值。
短句来源
更多       
  成骨不全
     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
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。
短句来源
     X-ray examination and family-line investigation in 32 cases of osteogenesis imperfecta
     32例成骨不全症X线检查及家系调察分析
短句来源
     Objective To study the gene mutation of collagen, type Ⅰ, alpha 1(COL1A1) associated with the clinical characterization of a Chinese family with type I osteogenesis imperfecta (OI).
     目的探讨一个成骨不全家系的COL1A1基因的突变位点及其与临床特征的关系。
短句来源
更多       
  “osteogenesis imperfecta”译为未确定词的双语例句
     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
     Results (1) A family was described in which hereditary osteogenesis imperfecta occurred in 5 generations. Forty two patients (18 males,24 females) ranged in age from 10 months to 67 years.
     结果(1)一家系五代42例(男18例,女24例)患病,年龄10个月至67岁。
短句来源
     Cardiopulmonary fitness and muscle strength in patients with osteogenesis imperfecta type I
     I型骨生成缺陷患者的心肺适应性和肌力
短句来源
     An investigation on clinical radiological diagnosis of hereditary osteogenesis imperfecta(a report of 42 patients in a family)
     遗传性成骨不全临床及X线诊断探讨(附一家系42例报告)
短句来源
     Analysis on characteristics of perinatal osteogenesis imperfecta in China
     中国先天性成骨不全围产儿特征分析
短句来源
更多       
查询“osteogenesis imperfecta”译词为用户自定义的双语例句

    我想查看译文中含有:的双语例句
例句
为了更好的帮助您理解掌握查询词或其译词在地道英语中的实际用法,我们为您准备了出自英文原文的大量英语例句,供您参考。
  osteogenesis imperfecta
Surgical treatment of the femur in osteogenesis imperfecta with intramedullary elongating rods
      
Beitrag zur Lehre von der Osteogenesis imperfecta tarda
      
Femurosteosynthesen mit dem Teleskopnagel nach Bailey-Dubow bei Osteogenesis imperfecta
      
Simultaneous Bilateral Tibial Tubercle Avulsion Fractures in a Boy with Osteogenesis Imperfecta
      
Treatment of children with osteogenesis imperfecta
      
更多          


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。

X-ray examination and family-line investigation were performed in 32 cases of osteogenesis imperfecta, suggesting that the modes of inheritance of the disease include autosomal dominant inheritance, autosomal recessive inheritance and sporadic cases caused by gene mutation. The authors found that the long bone X-ray changes of the patients in this series, besides short-thick, thin-long and saccular types, included 3 cases that were excluded from the above three types, and considered it necessary to add...

X-ray examination and family-line investigation were performed in 32 cases of osteogenesis imperfecta, suggesting that the modes of inheritance of the disease include autosomal dominant inheritance, autosomal recessive inheritance and sporadic cases caused by gene mutation. The authors found that the long bone X-ray changes of the patients in this series, besides short-thick, thin-long and saccular types, included 3 cases that were excluded from the above three types, and considered it necessary to add another type, or thin-cortical type, to Cao'S classification.

对32例成骨不全患者进行了家系随访调察和X线检查,提出本病的遗传方式为常染色体显性遗传、常染色体隐性遗传,以及基因突变引起的散发病例。发现本组病例长骨的X线改变除粗短型、细长型及囊型外。有3例不能归属以上3型。认为应在曹氏分类法的基础上,再补充一型,即薄皮质型。

 
<< 更多相关文摘    
图标索引 相关查询

 


 
CNKI小工具
在英文学术搜索中查有关osteogenesis imperfecta的内容
在知识搜索中查有关osteogenesis imperfecta的内容
在数字搜索中查有关osteogenesis imperfecta的内容
在概念知识元中查有关osteogenesis imperfecta的内容
在学术趋势中查有关osteogenesis imperfecta的内容
 
 

CNKI主页设CNKI翻译助手为主页 | 收藏CNKI翻译助手 | 广告服务 | 英文学术搜索
版权图标  2008 CNKI-中国知网
京ICP证040431号 互联网出版许可证 新出网证(京)字008号
北京市公安局海淀分局 备案号:110 1081725
版权图标 2008中国知网(cnki) 中国学术期刊(光盘版)电子杂志社