目的探讨不良妊娠史的细胞遗传学特点。
Objective: to investigate the characteristics of abnormal gestation and birth by cytogenetic study.
目的探讨不良生育史与细胞遗传学的关系。
Objective To investigate the relationship between nabnormal child-bearing history and cytogenetics.
在细胞遗传学中，镶嵌性有时也称为混倍体。
In cytogenetics, mosaicism is also sometimes referred to as mixoploidy.
它的结构、形态、功能是细胞遗传学中的核心内容。
Their structure, conformation, function are the cores of cytogenetics.
结论BMSC具有独特的细胞遗传学和免疫学特征。
Conclusion BMSC had unique cytogenetic and immunologic characteristics and provided a base for further investigation on purifying cells.
提示细胞遗传学对自发流产夫妇的临床诊断有很重要价值。
This paper showed that cytogenetics analysis is important for diagnosing the cases with spontaneous abortion.
目的探讨共济失调毛细血管扩张症的细胞遗传学异常特点。
Objective to investigate the characteristics of the cytogenetic anomalies of ataxia telangiectasia.
生物化学、生态学概论、植物学、细胞遗传学、分子遗传学……
Biochemistry, General Ecology, Botany, Cell Genetics, Molecular Genetics…
目的：研究再生丝素膜对大鼠真皮细胞生长和细胞遗传学的影响。
Objective: To investigate the effects of regenerated silk fibroin films on the growth and cytogenetic property of SD rat dermal cells.
两组间血液学缓解和细胞遗传学缓解总有效率差异均有统计学意义。
Between the two groups, the total effective rates of the hematologic remission and cytogenetic response was significant difference.
在细胞遗传学的临床与科学研究中，染色体分析是一项很重要的任务。
During the clinical and scientific research of cell genetics, the analysis of chromosome is an important task.
现在它已经成为细胞遗传学和细胞分类学上的一个最通俗基本的方法。
Now it has become one of the most popular basic technique in cell genetics and cell taxonomy.
结论：迁延照射造成的细胞遗传学损伤较一次照射严重，且修复缓慢。
CONCLUTION: There were more severe cytogenetic damage and slower repair in continual exposure to radiation than in a single irradiation.
目的探讨急性髓系白血病-M4、M5亚型的细胞遗传学、免疫表型特征。
Objective To study the cytogenetic and immunophenotype features in acute monocytic leukemia(M5) and acute myelomonocytic leukemia(M4).
结果：80 %患者达到血液学缓解，32 %患者产生细胞遗传学反应。
Results: 80 % of the patients reached the haematological alleviation, 32 % of the patients occurred cytogenetical reaction.
引起男性不育因素很多，大量研究已经表明男性不育与细胞遗传学异常有关。
Many factors can result in male infertility, and a number of studies have indicated that reproductive difficulties are associated intimately with cytogenetic abnormalities.
FISH技术在肿瘤生物学研究及临床细胞遗传学、出生前诊断等被广泛应用。
Making the most of M-FISH techniques in cancer research and preimplantation genetic diagnostics.
方法染色体G显带后按人类细胞遗传学国际命名体制（ISCN）进行核型分析。
METHODS G banding of chromosomes and then karyotype were analysized with an international system for human cytogenetic nomenclature (ISCN).
他们脱颖而出以及描述和单独的疾病的基础上，其临床，免疫和细胞遗传学特性。
They stand out as well-described and separate disorders on the basis of their clinical, immunophenotypic and cytogenetic properties.
结论本实验结果表明FISH在检测染色体畸变中比细胞遗传学核型分析方法敏感。
Conclusion The study showed that FISH was more sensitive than traditional cytogenetics in detection of chromosome aberrations.
随着分子细胞遗传学技术的应用，必将使体细胞变异在作物改良中发挥巨大的作用。
Somaclonal variation will play an important role in crop improvement with utilization of molecular cytogenetic techniques.
目的探讨急性白血病合并严重血小板增多症的细胞遗传学特点及其临床和实验室特征。
Objective To investigate the cytogenetic features as well as clinical and laboratory criteria of acute leukemia complicated with severe thrombocytosis.
双色FISH技术为评估基因的缺失提供了特异、敏感、直观的分子细胞遗传学证据。
Dual FISH technique provides specific, sensitive and direct evidence for molecular cytogenetic evaluation of gene deletion in tumors.
染色体图像分析是细胞遗传学研究的重要课题之一，它对人类疾病的诊断具有重要意义。
Chromosome image analysis is one of the essential tasks in cytogenetics, especially in genetic syndrome diagnosis.
目的研究慢性髓细胞白血病急变期(CML -BC)细胞遗传学及分子遗传学改变。
Objective to study the changes of cytogenetics and molecular genetics in chronic myeloid leukemia blast crisis (CML-BC).
对小麦-华山新麦草附加系H20和代换系H1的抗病性及分子细胞遗传学进行了研究。
The molecular cytogenetics and disease resistance of addition line H20 and substitution line H1 from wheat-P.
前言：在人类细胞遗传学中，荧光分子技术的出现带来了一些染色体研究和诊断的新方法。
Introducetion: in human cytogenetics, the advent of fluorescence molecular techniques has brought forth new procedures for chromosome investigation and diagnosis.
材料与方法：回顾性分析23例经细胞遗传学检查证实的21三体综合征的脑部ct表现。
Materials and Methods: Cerebral ct findings in 23 cases with 21 trisomy syndrome, proved by cytogenetics, were retrospectively analyzed.
材料与方法：回顾性分析23例经细胞遗传学检查证实的21三体综合征的脑部ct表现。
Materials and Methods: Cerebral ct findings in 23 cases with 21 trisomy syndrome, proved by cytogenetics, were retrospectively analyzed.
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