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- Chromosomal translocation is a kind of common chromosomal abnormality. 染色体易位是常见的染色体结构异常。
- Chromosomal disorder: Syndrome caused by chromosome abnormality. 染色体疾病:因染色体的异常导致的症候。
- Chromosomal disorder: Syndrome caused by chromosome abnormality. 染色体疾病:因染色体的异常导致的症候。
- 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。
- "One of the main reasons why IVF doesn't work is chromosomal abnormality," said Fishel. 生育专科经过了长期的探索，找到一种途径来检测受精卵或者胚胎以找出主要的异常染色体。
- Objective: To investigate the relationship between chromosomal abnormality, AZF microdeletion and azoospermia. 目的研究染色体异常及Y染色体AZF微缺失与无精子症的关系。
- Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis. 方法染色体检查排除染色体病,采用荧光光度计检测。
- Objective: To investigate the correlation of spermatogenesis impediment with chromosomal abnormality and with the deletion of DAZ gene. 摘要目的：探讨染色体核型异常和DAZ基因缺失与生精障碍的关系。
- Conclusion Chromosomal abnormality is the main factor that causes spontaneous abortion, teratogenic, mental retardation, female primary amenorrhea. 结论染色体异常是引起自然流产、畸胎、智力低下、女性原发闭经的重要原因。
- Objective:To investigate the correlation of chromosomal abnormality with the azoospermia and to study the meaning of the karyotype analysis in azoospermis. 目的应用细胞遗传学方法对无精子症患者进行分析,探讨染色体核型异常与无精子症的关系以及对无精子症进行染色体分析的意义。
- Fourty-four (10.6%) of subjects were found to have chromosome abnormality. 发现44例患者有染色体异常，频率为10.;6%25。
- Structural chromosomal abnormality is due to chromosome breakage with re-arrangement of fragments during repair. 结构染色体异常是由于断裂染色体在修复时重新排列所致。
- Underlying chromosomal abnormalities, such as trisomy 13, or maternal diabetes mellitus are possible causes, but some cases are sporadic. 潜在的染色体异常,例如三倍体13，或母亲的糖尿病也是可能的原因。
- Objective To discuss the correlation between sex chromosomal abnormalities and gonadal dysgenesis. 目的探讨性染色体异常对性腺发育的影响。
- Objective To investigate the chromosomal abnormalities and fusion genes of childhood acute myeloid leukemia(AML). 目的了解儿童急性髓细胞性白血病(AML)染色体及相关融合基因的变化。
- In this study, we used cytogenetic methods to identify the chromosomal abnormalities in patients with autism. 目前来说，自闭性疾患的盛行率大约0.;1~0
- Hyperdiploid chromosome abnormality was seen in 5(5/14) untreated patients with psoriasis and significantly higher than normal. 5例(5/14)未经治疗的银屑病患者外周血淋巴细胞染色体的超二倍体明显高于正常人。
- Doctors extract a cell from an embryo and test it for chromosomal abnormalities. 医生从胚胎中取出一个细胞，并且检测这个细胞是否有染色体遗传。
- Conclusion: chromosomal abnormalities play an important role in oligospermia and azoospermia. 结论染色体异常是导致少、弱精子及无精子症的重要因素之一。
