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1.12 cases of first reported chromosomal abnormality in the world
12例世界首报异常染色体核型分析收藏指正
2.Study on the Method of Screening Fetal Chromosomal Abnormality by Ultrasound
超声筛查胎儿染色体异常的研究收藏指正
3.The author thinks that chromosomal abnormality is of importance to caus- ing spontaneous abortion and puts foward a series of proposals on eugenic.
结合文献,对自然流产与染色体异常的发生率、病因等加以探讨,并提出一系列优生建议。收藏指正
4.ObjectiveA deletion of the long arm of chromosome 20 (del(20q) or 20q-) is the most frequent cytogenetic finding in malignant hematologic diseases with abnormalities of chromosome 20. In malignant hematologic diseases with a solitary chromosomal abnormality, 20q-represents the second most common structural abnormality after the Philadelphia chromosome.
恶性血液病中20号染色体最常见的异常是其长臂的部分缺失[del(20q)或20q-]。 在伴有单一染色体异常的恶性血液病中,20q-是发生率仅次于Ph染色体的第二个最常见的结构异常收藏指正
5.All the fetuses were followed up. Results The incidence of EIF was 0.73% in the normal group, and 1.61% in the fetuses with malformation or chromosomal abnormality. But there was no significant difference between the two groups (P>0.05).
结果①正常孕妇人群中胎儿EIF发生率为0.73%,与畸形胎儿或染色体异常胎儿EIF发生率1.61%,比较没有明显统计学意义(P>0.05);收藏指正
6.The clinical manifestation, hematologic abnormalites,AML?1?ETO chemeric gene and therapeutic response in twenty?three acute myelocytic leukemia patients with t(8;21) chromosomal abnormality were observed. The results showed that AML?1?ETO gene can be regarded as a molecular marker of acute myelocytic leukemia subtype M??2b?.
对23例t(8;21)阳性急性粒细胞白血病患者进行临床观察,结果表明∶AML1-ETO融合基因可作为急性粒细胞白血病M2b亚型的分子标志物;收藏指正
7.Molecular Cytogenetic Detection of Minute Chromosomal Structural Abnormality on the Chromosomal Terminal Regions
染色体末端微小结构异常的分子细胞遗传检测收藏指正
8.First Case Associated with Chromosomal Structural Abnormality 45,X,ter rea(X; 10) (p22;q26)
染色体结构异常45,X,ter rea(X;10)(p22;q26)首例报告收藏指正
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