选择已经定位染色体的SSR引物对单染色体进行PCR扩增，根据得到的分子标记进行单染色体的鉴定。
Select the SSR primer whose colorant layer is located to do PCR augmentation to the monosome, and certificate the monosome according to the gained molecular label.
尽管这最近鉴定出的遗传基因广泛存在于人体的23对染色体中，但它们关系的功能：都主要体现在学习上。
Though the newly identified genes are located in far-flung regions on the 23 human chromosomes, they are related in function: most play a role in learning.
结合这两个种的染色体倍性鉴定、序列分析和栽培观察实验，初步确定划分为两个种。
Acoording the ploidy analysis of chromosome, sequences and the survey of cultivation in field, Opisthopappus is primarily divided into two species.
经基因组原位杂交鉴定，BC1F4代中有披碱草的染色体组或染色体片段。
The genomic in situ hybridization showed that there are chromosomes or chromosome fragments of Elymus dahuricus in BC1F4.
传统的带型技术很难鉴定牡蛎的染色体。
Chromosome identification by traditional banding technique has been difficult in oysters.
结论FISH技术是染色体、染色体畸变鉴定和染色体上特殊序列定位的重要检测方法。
Conclusion FISH is a versatile technique for identifying chromosomes, detecting chromosomal abnormalities or determining the chromosomal localization of specific sequence.
方法：筛选出患长qt综合征1型的家庭成员，并鉴定KCNQ1基因中一个常染色体显性遗传突变基因(R190 Q)。
Methods We screened a family affected by long-QT syndrome type 1 and identified an autosomal dominant missense mutation (R190Q) in the KCNQ1 gene.
结论此10个X染色体sTR位点有较高的个体识别率，在个体识别和女孩亲权鉴定中有较高应用价值，对疾病相关研究有重要意义。
Conclusion The 10 X-chromosomal STR loci are appropriate for individual identification and paternity testing of a female child as well as for studies on related diseases.
目的：鉴定用于肿瘤比较基因组杂交(CGH)微阵列细菌人工染色体(BAC)克隆的质量。
Objective To evaluate the quality of BAC clones for CGH microarrays in the detection of tumors.
研究人员运用基因制图技术鉴定了2号染色体上的一小段DNA，而通常认为致病基因就存在于该染色体。
Using gene-mapping techniques, the researchers identified a small stretch of DNA on chromosome 2, where the disease-causing gene was thought to reside.
端粒克隆、着丝粒克隆以及重叠群之间空缺的大小都经过粗线期染色体荧光原位杂交鉴定。
BAC clones corresponding to telomeres, as well as to the centromere position and the gap sizes between contigs, were determined by BAC-pachytene chromosome fluorescence in situ hybridization (FISH).
目前仅有少数含有调节基因的染色体大致位点和可能的调控元件得到鉴定。
So far only a few crude chromosomal locations which should contain these regulatory genes and some putative regulatory elements have been identified.
DYS391和DYS393的X染色体扩增产物对法医学鉴定结论有误导可能性。
The co-amplification of the X-loci in DYS391 and DYS393 may mislead the forensic conclusion.
目的对小花鬼针草染色体核型等进行研究，为研究该种鉴定、起源、演化、良种培育等提供必要的细胞学资料。
OBJECTIVE To study the evolution, identification and fine seeds selection through Bidens parviflora chromosome number, karyotype and volume.
结论此10个X染色体sTR位点有较高的个体识别率，在个体识别和女孩亲权鉴定中有较高应用价值，对疾病相关研究有重要意义。
Conclusion The 10 X-chromosomal STRs loci are appropriate for individual identification, for paternity testing involving a female child, and for studies on related disease.
其他的候选基因也鉴定出来并定位到特定的染色体区域上。
Other candidate genes were also identified and assigned to specific chromosome regions.
现针对颅内动脉瘤的易感基因鉴定、候补基因分析及染色体基因座的连锁研究等遗传学方面的最新进展予以综述。
This article mainly reviews the identification of the susceptibility genes, the analysis of candidate genes and the mapping of chromosomal loci with…
摘要目的探讨y染色体微缺失和突变时，两男性个体间的全同胞关系鉴定。
Abstract: Objective To explore the identification method of full sibling between two males with microdeletion and mutation of Y chromosome.
目的：探讨X染色体s TR基因座独特的遗传方式在同胞亲缘关系鉴定中的应用。
Objective: To study the application of specific genetic pattern of X-chromosome STR loci in siblings' identification.
其中特别侧重介绍了该所在综合应用有利于精确鉴定外源染色体或其片段的各种方法技术方面的经验体会。
The ideas and experience are highlighted in the combined utilization of various methods and techniques for precise identification of alien...
其中特别侧重介绍了该所在综合应用有利于精确鉴定外源染色体或其片段的各种方法技术方面的经验体会。
The ideas and experience are highlighted in the combined utilization of various methods and techniques for precise identification of alien...
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