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- Methods: TC199 low level of folic acid cultivation method was performed to analyse both the frequency and the distribution of chromosome fragile sites in 31 habitual abortion couples. 方法采用低叶酸TC199培养诱导法,观察了31对染色体核型无异常的习惯性流产夫妇染色体脆性位点,并观察了脆性位点的分布。
- Surrounding blood chromosome fragile sites study on colorectal carcinoma 结直肠癌患者外周血染色体脆性位点研究
- Analysis of chromosome fragile sites in the habitual abortion couples 习惯性流产夫妇染色体脆性位点的观察
- A Comparison of Chromosome Fragile Sites in Elderly and Young People 老年人与青年人染色体脆性位点的比较
- STUDIES ON THE CHROMOSOME FRAGILE SITES OF PATIENT WITH NPC AND IgA/VCA ANTIBODY POSITIVE INDIVIDUALS 鼻咽癌患者和EB病毒IgA/VCA抗体阳性者染色体脆性部位研究
- A Study of Chromosome Fragile Site and Clinical Manifestation of Children Acute Leukemia 小儿急性白血病染色体的脆性部位与临床分析
- Expression of Chromosome Fragile Site in Peripheral Lymphocytes in Benign and Malignant Gastric Diseases and Its Role in the Genesis of Gastric Cancer 胃良恶性疾病外周血淋巴细胞染色体脆性位点表达与胃癌的发生
- Chromosome Fragile Sites 染色体脆性位点
- THE STUDY OF CHROMOSOMAL FRAGILE SITES IN CHRONIC GLOMERUIONEPHRITIS URAEMIA 慢性肾炎尿毒症患者染色体脆性位点的初步研究
- chromosome fragile site 染色体脆弱位点
- Objective:To investigate the roles of the chromosome aberrations and fragile sites in the nasopharyngeal cancer (NPC) family. 目的:探讨染色体畸变和脆性部位表达在鼻咽癌家族发病中的意义。
- The mental retardation is correlative with the chromosome aberration and the fragile site expression rate. 提示精神发育迟滞与染色体的畸变率和脆性部位的表达率有一定的相关性。
- Conclusion: The mental retardation is correlative with the chromosome aberration and the fragile site expression rate. 结论:提示精神发育迟滞与染色体的畸变率和脆性部位的表达率有一定的相关性。
- Chromosomal fragile sites 染色体脆性位点
- The family members with certain common fragile sites probably do not indicate an elevating risk for NPC. 某些常见型脆性部位的检出可能不代表家族成员患鼻咽癌风险升高。
- Methods:From Oct,2002 to Dec,2004,204 children with different degree MR,X-chromosome fragile site were detected by low folic acid cultivation. 方法:对2002年10月-2004年12月该院门诊和病房不同程度的智力低下病人204例进行了外周血淋巴细胞低叶酸培养方法诱导脆性位点脆性X染色体研究。
- Mr James Bainbridge, who leads the surgical team, said: "It is very encouraging that we can deliver genes to an extremely fragile site in the eye without complications. 领导手术队伍的JamesBainbridge说:“我们能够将基因导入眼睛的一个极度易碎的部位,而且没有并发症,这是很让人鼓舞的。”
- The FMR-1 gene mutation and Xq27.3 fragile site among 233 non-specific mentally retarded children were investigated in our genetic counseling department and two special educational schools by PCR, Southern Blot hybridization and cytogenetic methods. 采用PCR、Southern Blot印迹杂交及细胞遗传学方法;对233名原发性智力低下患儿进行了FMR-1基因的突变分析和Xq27.;3脆性位点检查。
- This glass plate is very fragile. 这个玻璃盘子很容易碎。
- A Study of the Fragile Sites in Autism 儿童孤独症的染色体脆性位点研究