Chromosome 5

Chromosome 5 might exist many new genes locations related with metastasis of colorectal carcinoma .

5号染色体上可能存在多个与大肠癌转移相关的新基因位点。

SMA is caused by an abnormal version of a gene on chromosome 5 .

脊髓性肌肉萎缩症是由5号染色体上的一个基因异常造成的。

Analysis of the fine physical map of chromosome 5 of Saccharomyces cerevisiae

啤酒酵母五号染色体精细物理图谱分析

Study of Microsatellite Instability on Chromosome 5 in Leukemia and MDS

5号染色体微卫星不稳定性与白血病和骨髓增生异常综合征关系的研究

The disease gene is exactly located on the chromosome 5 and chromosome 12 through parameter and non-parameter linkage analysis .

综合运用参数和非参数连锁分析，将致病基因定位到5号染色体和12号染色体上。

Chromosome 5 is distinguished by a proximal knob .

第5染色体的特点是有一个近侧的节结。

Meanwhile , there probable exist QTLs on chromosome 5 , 6 , 9 and 14 , their LOD values reached above 1.5 . The results were in accordance with professor Zhao obtained .

另外，在第5、6、9和14条染色体上也可能存在QTLs，它们的LOD值均达到1.5以上，此结果与赵卫东的定位结果吻合。

The chromosome observation on 5 species of rare plants of China

我国5种珍稀植物的染色体观察

A Case Report of Chromosome 3 / 5 Balanced Translocation

染色体3/5平衡易位一例报告

Among 19 cases autosomal abnormal are 14 cases , sex chromosome abnormal are 5 cases .

其中，常染色体异常14例，性染色体异常5例。

Two pairs of epistatic QTLs were detected on chromosome 3 , 5 and 7 with significant epistatic effects .

在第3、5、7染色体上检测到两对互作位点。

Silver staining PCR-SSCP method was used to detect microsatellite instability ( MIN ) at 4 loci on chromosome 2 , 5 、 17 in paraffin-embedded gastric carcinoma tissues .

应用银染PCR-SSCP方法检测30例常规石蜡包埋胃癌组织第2、5、17号染色体4个位点的微小卫星DNA不稳定性（MIN）。

Objective A follow-up study of chromosome aberrations in 5 victims accidentally exposed to 60 Co - γ - rays 12 years ago was performed to give assessments of the late effect of radiation .

目的对上海6255名60Co源事故受照射者12年后的染色体畸变进行追踪观察，为辐射远后效应评价提供依据。

Four QTLs of rows number per ear were detected on chromosome 2 , 5 , 6 and 6 , which explained phenotypic variance 22.74 % , each explained 4.19 % - 8.79 % .

对穗行数，检测到了4个QTL，分别位于第2,5,6染色体上，共解释表型变异的22.74%。

Conclusion The distribution of allele frequencies of 8 STR loci on chromosome 11 and 5 STR loci on chromosome 19 was consistent with the Hardy Weinberg equilibrium and the highly genetic polymorphism was observed in Chinese Han population .

结论11号染色体的8个STR位点和19号染色体的5个STR位点在中国汉族人群中有较好的多态性，其基因频率分布符合Hardy-Weinberg平衡。

Diagnosis of the disease was made mainly by examination of white blood cell count and neutrophilic percentage of the ascitic fluid . Among 85 benign cases , chromosome numbers of 5 cases ranged from diploid to tetraploid , and that of the others were diploid or not observed .

该病诊断要点是依据腹水检查中的白细胞计数及中性白细胞所占百分率。85例良性胸腹水检查出现二倍体至四倍体染色体5例，其余为二倍体或未见分裂相；

A reciprocal translocation between 6 and 11 was further confirmed by chromosome painting technique in 5 cases .

全染色体涂染技术分析也证实5例患者6号和11号染色体之间发生了相互易位。

The Chromosome Numbers of 3 5 Forage Species and Their Geographical Distributio

35种国产饲用植物染色体数目的观测

The disease cause by the mutation in human beta globin gene cluster , which located on chromosome 11 and includes 5 functional genes and 1 pseudo gene .

β珠蛋白基因簇位于人11号染色体上，包含5个功能基因和1个假基因，这些基因的突变导致血红蛋白合成异常而发病。

Methods Karyotype analysis was performed by R banding technique and chromosome painting with whole chromosome 3 and 5 painting probes .

方法R显带染色体核型分析和染色体涂染分析确定t（3；5）（q25；q34）存在。

Loci showed LOH frequency from 50 % to 59 % , three of them are located on chromosome 3 , and 1 on chromosome 5 and 11 ;

5个位点LOH频率介于50%～59%，其中3个在3号染色体，5号和11号染色体各1个位点；

The results obtained by counting 141 mitotic cells showed the chromosome number in the chromosome set ranged between 5 20 , and 14 18 chromosome were clearly predominant .

通过对141个分裂像的观察分析，结果表明细粒棘球蚴染色体组的染色体数在5～20条之间，14～18条占明显优势。

QTLs of the agronomic traits were detected in relative chromosome . A total of seven QTLs contributing to six agronomic traits was identified and located on chromosome 5 , 7 , 8 and 9 , respectively .

在可能检测到抗性QTL的染色体上还进行了农艺性状的定位，检测到7个QTL，涉及6个性状，分别位于第5、7、8和9染色体上。