1) chromosome structural aberration
染色体结构异常
1.
Objective To delineate the chromosome structural aberration in a case of chromosome translocation by fluorescence in situ hybridization(FISH) technique and precisely identify the breakpoints.
目的 应用荧光原位杂交技术对 1例染色体结构异常患者进行分析 ,阐明结构异常性质 ,并精细定位断点。
2.
Objective To analyze the chromosome structural aberration in a case of unbalanced chromosome translocation by fluorescence in situ hybridization technique.
方法 对经细胞遗传学提示的染色体结构异常的病例,选用1、18号染色体探针池进行涂染。
2) Chromosomal sub-microstructure abnormality
染色体亚微结构异常
4) 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。
5) 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。
6) 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。
补充资料：染色体结构异常
染色体结构异常
参见"染色体畸变"。
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