euchromosome

euchromosome

1. In 146 cases of chromosomes aberrance,the rate of abnormal eu-chromosome number and abnormal euchromosome structure was 4. 8% (7/146) and 29. 5% (43/146).

146例外周血染色体异常核型中常染色体数目异常占4.8%(7/146); 常染色体结构异常占29.5%(43/146);

2. It provides an experiment basis for combining highly genetic specificity of human euchromosome STR (Short Tandem Repeat, STR) with Y- chromosome STR study.

为结合具有高度遗传特异性的人类常染色体及Y染色体短串联重复序列（Short Tandem Repeat, STR）的研究，构建墓葬血亲关系深层次研究奠定了基础。

3. Keywords likelihood ratio（LR）;grandparents and grandchild;euchromosome STR;obliged gene;

似然率;祖孙;常染色体STR;生父基因;

4. In transmissibility myopia, high myopia belongs to euchromosome recessive heredity, general myopia belongs to much factor hereditary disease.

在遗传性近视眼中,高度近视属常染色体隐性遗传,一般近视属多因子遗传病。

5. Keywords Health protection before marry;Euchromosome viewy genetic ill;Filial generation be taken bad;

婚前医学体检;常染色体显性遗传病;子代发病;

6. Consider as what recessive heredity causes euchromosome to high myopia.

对于高度近视则认为是常染色体隐性遗传引起的。

7. euchromosome STR

常染色体STR

8. Kinship Analysis of Grandparents and Grandchild with STR on Euchromosome

常染色体STR祖孙亲缘关系鉴定分析

9. Methods: Using site-specific primers for 24 euchromosome STR loci, the individual genome DNA of 66 cases of diad paternity testing were typed after synchronized PCR and PAGE followed by silver staining.

方法 :应用PCR同步扩增 2 4个常染色体STR基因座 ,PAGE电泳分型 ,完成二联体亲子鉴定 6 6例。

10. This disease by euchromosome recessive heredity.

本病由常染色体隐性遗传。

11. The heredity that seldom counts case of illness passes euchromosome, euchromosome is genetic person also can have anaemia.

极少数病例的遗传是通过常染色体的，常染色体遗传者则亦可有贫血。

12. Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色体隐性遗传病。

13. The paternity in diad paternity testing cases can be successfully confirmed or excluded after DNA typing of 24 euchromosome STR loci simultaneously.

经 2 4个常染色体STR基因座检测 ,能确切地认定或排除亲生关系 ,得出正确的鉴定结论

14. Results: In 146 cases of chromosomes aberrance,the rate of abnormal eu-chromosome number and abnormal euchromosome structure was 4. 8% (7/146) and 29. 5% (43/146).

结果:146例外周血染色体异常核型中常染色体数目异常占4.8%(7/146);常染色体结构异常占29.5%(43/146);

15. 9. Results: In 146 cases of chromosomes aberrance,the rate of abnormal eu-chromosome number and abnormal euchromosome structure was 4. 8% (7/146) and 29. 5% (43/146).

结果:146例外周血染色体异常核型中常染色体数目异常占4.8%(7/146);常染色体结构异常占29.5%(43/146);收藏指正

16. Conclusion: The paternity in diad paternity testing cases can be successfully confirmed or excluded after DNA typing of 24 euchromosome STR loci simultaneously.

结论：经24个常染色体STR基因座检测，能确切地认定或排除亲生关系，得出正确的鉴定结论。

17. Denaturation of nucleus of liver beans shape is the familial sex disease that the cupreous metabolization obstacle with a kind of recessive and genetic euchromosome causes.

肝豆状核变性是一种常染色体隐性遗传的铜代谢障碍引起的家族性疾病。