Screening the sensitive deafness genes in newborn is imminent.

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By microarray analysis and linkage analysis, we identified the gene responsible for the Ibc mutant, and investigated its expression patterns. We also cloned the full-length of the candidate gene by RACE and carried out preliminary function verifications.

通过基因芯片筛查与连锁分析，本研究筛选并克隆了lbc突变的的候选基因，同时分析了突变基因的表达特征，并对该基因进行了初步的功能研究。

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Study on Genes Related to Gastric Carcinoma Metastasis by LCM Relationship between Abnormal Expression of E-cadherin-catenin Complex and Biological Behaviors of Gastric Carcinoma

LCM技术体系的建立及胃癌转移相关基因的筛查E-cadherin-catenin复合体表达与胃癌生物学行为的相关研究

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Objective: To screen the BSEP gene in intrahepatic cholestasis of idiopathic infantile hepatitis patients.

目的：对特发性婴儿肝炎肝内胆汁淤积患儿的BSEP基因进行筛查，初步探讨胆盐输出泵基因与特发性婴儿肝炎肝内胆汁淤积的关系。

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The genes showing altered expression related to apoptosis induced by As_ ( 2) O_ ( 3) were screened by cDNA microarray, and the results were confirmed by real-time quantitative PCR.

用cDNA基因芯片筛查与As2O3诱导凋亡发生相关的基因，并用实时定量PCR技术验证结果。

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SNP Screening in the Related Candidate Gene for IMP Contents of Chicken and Its Application in Assessment of Genetic Structure of Indigenous Chicken Breeds

鸡肉IMP含量相关候选基因SNP筛查及其用于地方鸡种群体遗传结构分析的研究

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Screening gene mutations of the mitochondrial tRNA~ Lys in familial diabetes mellitus

中国人家族性糖尿病人群中线粒体tRNA~（Lys）基因突变筛查

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Scanning of Differentially Methylated Genes Associated with Phenotype in CpG Islands DNA of Whole Genome between HBV Infected Monozygotic Twin Pairs

HBV感染后表型相关单卵孪生子基因组CpG岛差异甲基化基因的筛查

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Screening the WT1 Gene Mutations in 24 Cases of Wilms' Tumors

24例肾母细胞瘤WT1基因突变筛查

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Conclusion Multiple PCR technique is simple, accurate, rapid and feasible for the screening of deletional α-thalassemia in population of at high risk.

结论多重PCR法用于高发群体缺失型α-地贫基因的筛查，具有简便、准确、快速、实用的特点。

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Parallel Screening of Medical RNA Viruses on Genus Level by Microarray Technique

医学RNA病毒属水平基因芯片筛查技术的研究

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Real-time PCR results confirm that this microarray screening results are a true and reliable.

Real-time PcR结果证实本次基因芯片筛查结果真实、可靠。

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Screening for apolipoprotein E gene mutations in 4 patients with lipoprotein glomerulopathy

四例脂蛋白肾病患者载脂蛋白E基因突变筛查

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For the past few years, with the further of genetics research aimed to pathological myopia, the scholars utilize the techniques such as genome scan 、 candidate gene screening 、 linkage analysis to locate the related gene of pathological myopia and the candidate gene clone.

近年来，国内外学者对高度近视的遗传学研究进一步深入，已应用全基因组扫描和候选基因筛查、连锁分析等技术进行病理性近视相关基因定位和候选基因克隆定位工作。

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Results By PCR-RDB, nine people were proven to have typical phenotypes of β-thalassemia, which were not categorized into the sixteen known genotypes though. The β-globin gene mutations were characterized by PCR-reverse dot blot ( RDB).

结果运用PCR-反向点杂交技术进行基因筛查，发现9例具有典型β-地中海贫血表型特征，但不属于已知的16种β-地中海贫血突变类型。

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Proponents of universal prepregnancy genetic screening make a bold claim: If these tests were widely available, they could significantly reduce, and possibly eliminate, hereditary diseases.

全民孕前基因筛查的支持者大胆地声称：如果这些检测被广泛推广，将会大幅减少、甚至有可能消除遗传疾病。

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" It's sparking a lot of conversations," she said. "These are difficult issues for everybody."

“基因筛查激发了许多讨论，”她说，“对每一个人来说这些讨论都是艰难的问题。”

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Role of molecular screening for common fusion genes in the diagnosis and classification of leukemia

常见白血病融合基因筛查在白血病诊断与分型中的意义

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Screening and Expression of Associated Genes in Gastric Carcinoma

胃癌相关基因筛查及表达研究

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Screening for Causative Genes Involved in Children with Minimal Change Nephritic Syndrome

儿童微小病变型肾病综合征致病相关基因筛查

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Screening the γ-crystallin Genes in a Congenital Nuclear Cataract Family

一个先天性核性白内障家族的γ晶状体蛋白基因筛查

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