1) chromosomal abnormal behavior
染色体异常行为
1.
Observation of the variation of the chromosomal behavior in second Filial generation during meiosis is made on the hybrid of wheat -rye 5R/5A disomic substitution line and 6R/6A disomic substitution line, and the chromosomal abnormal behavior and the coherency with chromosomal translocation are analyzed.
所以,在减数分裂过程中出现单价体、多价体、落后染色体、微核等染色体异常行为,这些现象会影响染色体配对、交换,对研究染色体易位的形成能提供重要依据。
2) Abnormal chromosomal behavior
染色体行为异常
1.
Abnormal chromosomal behavior of root tip cells emerged when the NaCl concentration was more than 100 mmol/L.
结果表明,随着NaCl浓度的升高,旱稻的发芽率、发芽指数、活力指数逐渐降低;NaCl浓度高于100 mmol/L时,引起根尖细胞染色体行为异常,异常类型有微核、多核、染色体落后、染色体粘连、染色体桥、染色体断裂等。
3) chromosomal aberration
染色体异常
1.
The aim of study was to investigate the importance of chromosome aberration in differential diagnosis of eosinophilia and the chromosomal aberrations involved in patients with clonal eosinophilia.
为探讨染色体异常克隆在嗜酸性粒细胞增多症诊断和鉴别诊断中的意义及克隆性嗜酸性粒细胞增多症涉及的染色体异常,收集了65例嗜酸性粒细胞增多患者的骨髓标本,培养24小时,采用G显带进行核型分析。
2.
The chromosomal aberration was checked out in 46 cases from 389 related patients,ratio:11.
其中罗伯逊易位携带者 6例 ,平衡易位携带者10例 ,倒位携带者 4例 ,性染色体异常者 14例 ,先天愚型及发育异常者 12例 。
3.
To investigate chromosomal aberration and HPV18 E6,HPV18 E7 proteins expression in human embryonic esophageal epithelial cells transfected with HPV18 DNA during immortalization and malignant transformation.
[目的 ]研究HPV18DNA转染的人胚食管上皮细胞永生化及其恶性转化过程中的染色体异常和HPV18E6、HPV18E7蛋白表达情况。
4) chromosome abnormality
染色体异常
1.
The rapid diagnosis of common chromosome abnormality in prenatal diagnosis;
产前诊断中常见染色体异常的快速诊断
2.
This study was to explore the clinical significance of FLT3 internal tandem duplication (FLT3/ITD) in acute myeloid leukemia (AML) with chromosome abnormality.
本研究旨在探讨伴有染色体异常急性髓系白血病患者FLT3跨膜区内部串联重复突变检测的临床意义。
3.
Objective To investigate the frequency of chromosome abnormality in 415 infertile males.
目的研究中国人群男性不育患者的染色体异常频率分布。
5) Chromosome aberration
染色体异常
1.
Results There were 38 chromosome aberrations(29 women,9 men) in them,the abnormal rate being 3.
结果发现染色体异常核型38例,异常发生率为3。
6) Chromosome abnormalities
染色体异常
1.
Detection of common chromosome abnormalities in myelodysplastic syndrome with a panel fluorescence in situ hybridization;
组合探针荧光原位杂交检测骨髓增生异常综合征常见染色体异常
2.
Conclusion:Chromosome abnormalities was one of the main causes of primary amenorrhea.
结果在126例原发闭经患者中共检出染色体异常43例,异常检出率为34。
补充资料：异常行为
见越轨行为。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条