1.
To Identify the Deletion of Chromosome 13 in 17 Patients with Multiple Myeloma
17例多发性骨髓瘤患者13号染色体缺失的检测
2.
Utility of Fluorescence in Situ Hybridization in the Partial Deletion of Chromosome 13 in Multiple Myeloma
荧光原位杂交技术在检测多发性骨髓瘤患者13号染色体部分缺失中的应用
3.
Significance of Monosome 7 or Deletion of the Long Arm of Chromosome 7
单体7或7号染色体长臂缺失的意义
4.
simultaneous del(13q) and 14q32 rearrangement in 26.1%.
13号和14号染色体异常同时存在的检出率为26.1%;
5.
Significance of loss of heterozygosity chromosome 1 in hepatocellular carcinoma
肝癌1号染色体等位基因杂合性缺失及临床意义
6.
Loss of Heterozygosity on the Long Arm of Chromosome 6 in Peripheral T Cell Non-Hodgkin s Lymphoma;
T细胞非霍奇金淋巴瘤6号染色体长臂杂合性缺失的研究
7.
Study of Loss of Heterozygosity and Microsatellite Instability on Chromosome 7 in Leukemia;
急性白血病的7号染色体杂合性缺失和微卫星不稳定性研究
8.
Study of Microsatellite Instability and Loss of Heterozygosity on Chromosome 8 in Leukemia;
白血病患者8号染色体微卫星不稳定性和杂合性缺失的研究
9.
Advance of Studies on Loss of Heterozygosity of 17p and Tumor;
第17号染色体短臂杂合性缺失与肿瘤的研究进展
10.
Analysis of Loss of Heterozygosity and Microsatellite Instability of 3, 4 Chromosome in Human Squamous Carcinoma in Cervix
宫颈鳞癌3、4号染色体杂合性缺失与微卫星不稳定性分析
11.
Study on the Loss of Heterozygosity on Chromosome 3,7,8,9,17 in Clear Cell Renal Carcinoma
肾透明细胞癌3、7、8、9、17号染色体的杂合性缺失研究
12.
Screening the Chromosome Ⅰ Deficiency Stockes by Using Drosophila Pacing-Model
利用果蝇心功能衰竭模型筛选1号染色体缺失系
13.
Phosphatase and Tensin Homology Deleted on Chromosome 10 and Neural Development
10号染色体上缺失的磷酸酶与张力蛋白同源物基因与神经发育
14.
Deletions of Derivative Chromosome 9 in 138 Patients with Chronic Myeloid Leukemia
138例慢性髓系白血病衍生9号染色体缺失的研究
15.
Progresses on the genetic study of 22q11 deletion syndrome
22号染色体长臂近端微片段缺失综合征的遗传学研究
16.
Clinical and Experimental Studies of Derivative Chromosome 9 Deletion in Patients with Ph-positive Leukemia;
Ph+染色体白血病患者中衍生9号染色体部分序列缺失的临床和实验研究
17.
Chromosomal and Y chromosome microdeletion analysis in patients with oligozoospermia
男性少精子患者染色体和Y染色体微缺失检查
18.
If both of a pair of homologous chromosomes are missing, nullisomy results.
如果一对同源染色体都缺失了,称为缺体。