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   染色质阴性 的翻译结果: 查询用时:0.352秒
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染色质阴性
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  “染色质阴性”译为未确定词的双语例句
     X chromatin of two female patients were negative and the karyotypes of the abnormal X chromosome was 45,X/46,XX, the rate of 45,X was 1.2 ;
     2例女性患者X染色质阴性,染色体核型为45,X/46,XX, 45,X型发生率为0. 12%;
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  相似匹配句对
     CHROMATIN
     染色质
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     STRUCTURE OF CHROMATIN
     染色质的结构
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     PAS was negative.
     PAS阴性
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     The nuclei of late spermatids with elongated nucleus (steps 18, 19) and spermatozoa were PTA negative.
     至长形核的晚期精子细胞,其核内染色质呈PTA阴性
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     There were also 9 cases being false negative.
     阴性9例;
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  chromatin negative
A human XXY chromatin negative triploid culture has been found to have both the A and B isozymes of glucose-6-phosphate dehydrogenase, as well as an intermediately migrating AB (hybrid) band.
      
The X chromatin was positive and the Y chromatin negative in the 3 affected subjects.
      
None of the female patients with mental retardation was chromatin negative.
      
Testicular dysgenesis was proved on biopsy and he was sex chromatin negative.
      


This paper reports a family of male pseudohermaphroditism, in which three out of four children are pseudohermaphroditism, and their parents are both normal. The abnormal children are of normal male caryotype (46,XY), and the result of sex chromatin test is negetive, indicating that there is no chromosome aberration detected. Pedigree analysis shows this type of male pseudohermaphroditism is probably X-linked ressesive.

本文报导一个男性假两性畸型的家族,在这个家族中有4个男孩,其中有3个为男性假两性畸型,可是他们的双亲皆正常。这三个异常孩子的染色体组型都是正常的(46,xy),性染色质阴性,表明可能不是因染色体畸变所致。根据家谱分析,这种类型的男性假两性畸型可能属于X连锁隐性遗传。

The paper reported a case of sibling with imcomplete male pseadoher-maphroditism, The social sexuality of the sibling was female. But they had testes and no uterus and vigina. The periheral haemocyte Chromsome was 46xy. Thex Chromatin of oral adhersive cells was of negative. The grandmother and grandmother - in-law of the sibling were sisters. The parents of the sibling were cognative copulation. The coefficient of consanguinity was one-eighth. ( R = 1/8) Both of them were of hetero-cygous. There were two suffers...

The paper reported a case of sibling with imcomplete male pseadoher-maphroditism, The social sexuality of the sibling was female. But they had testes and no uterus and vigina. The periheral haemocyte Chromsome was 46xy. Thex Chromatin of oral adhersive cells was of negative. The grandmother and grandmother - in-law of the sibling were sisters. The parents of the sibling were cognative copulation. The coefficient of consanguinity was one-eighth. ( R = 1/8) Both of them were of hetero-cygous. There were two suffers among their children whowere of isozygoty. (R = l/4)This accorded with the autosome recessive heredity.

本文报道了在同胞姊妹中同时出现两位不完全性男性假两性畸形Ⅱ型的病例,两患者社会性别均为女性,但患者具有睾丸,无子宫及阴道,外周血细胞染色体核型分析为46xy、口腔粘膜细胞X染色质阴性,患者祖母与外祖母系亲姊妹,父母为近亲结合,亲缘系数r=1/8,均为杂合子,其子女8人中,有二位患者,为纯合型,占1/4,符合常染色体隐性遗传方式。

17 Cases of testicular deficiency from 1985 to 1986 are reported。Two main cli-nical types are classified according to the serum level of gonadotrophin:high gon-adotrophin type (14 cases) and the low one (3 cases)。The former was further classifiedinto three sub-groups based upon buccal smear,namely,chromatin positive Kline-felter's syndrome(3 cases),chromatin negative apparent type of Klinefelter's syndr-ome (9 cases)and testicular deficiency by other causes (Sertoli cell only syndrome 2cases)。The characteristic...

17 Cases of testicular deficiency from 1985 to 1986 are reported。Two main cli-nical types are classified according to the serum level of gonadotrophin:high gon-adotrophin type (14 cases) and the low one (3 cases)。The former was further classifiedinto three sub-groups based upon buccal smear,namely,chromatin positive Kline-felter's syndrome(3 cases),chromatin negative apparent type of Klinefelter's syndr-ome (9 cases)and testicular deficiency by other causes (Sertoli cell only syndrome 2cases)。The characteristic clinical manifestation,testicular biopsies and palmar-digitaldermatographic patterns are discussed and analyzed.

本文报告睾丸发育不全症17例。临床分型按血清促性腺激素水平分为高促性腺激素型(14例)及低促性腺激素型(3例)二大类。前者又按颊部粘膜涂片检查结果而分为:性染色质阳性克氏综合征(3例)性染色质阴性克氏征表现型(9例),以及其他原因的睾丸发育不全症(唯支持细胞综合征(2例)。作者就各临床型的特征,睾丸活检及掌-指纹理构型进行分析讨论。着重指出掌-指纹理中的弓形纹、桡向箕形纹及双箕斗形纹的高出现频率在辅助诊断性腺发育不全上是有帮助的。

 
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