即使技术允许，任何经基因筛检出的聋或矮宝宝是否能出生也是不确定的。
While it's technologically possible, whether any deaf or dwarf babies have been born as a result of PGD is uncertain.
基因筛查正快速成为一种有效手段，不仅运用于癌症诊断，而且也用于癌症治疗。
Gene screens are fast becoming a powerful tool, not just for diagnosing cancer but for treating it as well.
在解剖阴性者中进行分子基因筛查，对解释病因和SCD危险分层有重要作用。
Molecular genetic screening in negative autopsy cases can play an important role in explaining the cause of SCD and risk stratification of SCD.
杰克逊说，对可能要做父母的人进行全面的遗传基因筛检，可以避免很多疾病和痛苦。
Jackson says a comprehensive screening test for prospective parents could avert a lot of pain and suffering.
建议将此突变位点检测运用于遗传咨询、产前诊断、新生儿和不明原因感音神经性聋患者的基因筛查中。
It is suggested to utilize this detection for genetic counseling, prenatal diagnosis, and the genetic screening of neonates and the sensorineural hearing loss with unknown reason.
通过基因筛查技术可以筛选出那些女性的胎儿存在此种风险，并通过饮食补充或药物治疗来阻止酒精的影响。
The hope is that gene screening could ID women whose fetuses would be at-risk, and that dietary supplements or drugs could block alcohol’s effect.
孩子们可以接受基因测试以确认他们是否遗传了此变异，并且定期进行癌症筛检。
The children can receive genetic testing to find out if they have the mutation, and regular cancer screenings.
新的胚胎筛检技术称为基因组杂交比较，允许医生从几天大的胚胎上提取细胞。
The new screening tecnique, called comparative genomic hybridisation, allows doctors to remove cells from an embryo when it is a few days old.
利用最新的技术，科学家们将对该研究中的组织标本进行筛查以寻找早期动脉粥样硬化的易患变异基因。
Using the latest technology, scientists will screen tissue samples from the study looking for genetic variants that may predispose individuals to develop early atherosclerosis.
目的建立一种简便、准确和快速的筛查苯丙酮尿症突变基因的方法。
Objective to establish a simple, accurate and rapid method for screening of the mutant genes in phenylketonuria.
用退火控制引物(acp)的差异筛选分析法对该样本进行候选基因的初筛。
The pooled samples were initially screened for candidate genes for narcolepsy by differential display analysis using annealing control primers (ACP).
目的对广东地区汉族人群的甘露聚糖结合凝集素结构基因第一外显子第54位密码点突变（GGC54GAC）进行初步筛查。
Objective To screen the point mutation at the codon 54(GGC54GAC) in the first exon of the mannan binding lectin (MBL) gene in Hans from Guangdong.
对筛查出的多态性基因进行测序分析。
目的了解基因芯片技术在筛查正常或异常胚胎发育的相关基因表达变化中的应用价值。
Objective To investigate the role of gene chip technique in screening normal or abnormal developing embryo related genes.
现就近年来乳腺癌易感基因的遗传学研究及基因变异的筛查技术进展作一综述。
This review will address the research advancement in genetic studies of breast cancer susceptibility as well as the screening methods for gene mutations.
目的：观察单链构象多态性(SSCP)筛查akt2基因突变时凝胶配制的不同对筛查结果的影响。
Objective: To observe the effect of different gel preparation on detecting mutation of AKT2 gene by single-strand conformation polymorphism (SSCP).
Grifo说他不反对胚胎筛检用于选择有基因缺陷的宝宝，前提是父母已被告知利弊、风险、收益。
Grifo said he wouldn't oppose embryo screening to select a baby with a genetic defect if the parents have been informed of the pros and cons, risks and benefits.
目的：遗传性板层白内障家系致病基因的定位及突变筛查。
Objective: We tried to identify the genetic defect causing Hereditary lamellar Cataract.
目的：制备人类致病病毒属水平高通量筛查用基因芯片，并通过检测黄病毒属病毒初步验证其筛查效果。
Objective: to establish a high throughput DNA microarray method for rapidly screening human viral pathogens, and to verify its effectiveness by detecting Flavivirus.
该技术速度快，易于自动化，特别适合大量单碱基突变基因的筛查。
This method is characteristic of high speed, easy automation, and is especially suitable for high throughput screening.
结论：由于PCR -双酶切方法快速、简单、易操作，且特异性好，可作为CMT1A基因诊断的一种初筛方法。
CONCLUSION: Because of the speediness, simpleness and good specificity, the PCR combined with restriction enzyme digestion can be used as a primary screening in the gene diagnosis of CMT1A.
一个国际研究小组设计了一种检测方法来筛查和鉴别肿瘤生长抑制基因。
An international research team has developed a method for the screening and identification of tumour growth-suppressing genes.
结论：制作的基因芯片可准确识别嗜铬细胞瘤相关的基因突变，为筛查嗜铬细胞瘤基因突变提供一种快速的方法。
Conclusions: The gene chip could accurately identify genetic mutations related to pheochromocytoma, which could provide a quick method of screening genetic mutations in pheochromocytoma.
采用聚合酶链反应(PCR)方法扩增rho基因第1 ~ 5外显子和第1内含子基因片段，用直接dna测序法筛查rho基因突变。
Extron 1-5 of RHO gene was amplified by polymerase chain reaction (PCR), and the mutation of RHO gene was screened by direct DNA sequence measurement.
运用新方法在单个实验室中就可以筛查上千个基因。
The new method allows the screening of thousands of genes in a single laboratory experiment.
方法采用PCR - SSCP筛查与DNA直接测序的方法对12例okc进行PTCH基因突变的检测，其中2例为痣样基底细胞癌综合征(NBCCS)相关okc,10例为散发okc。
Methods PCRSSCP and DNA sequencing were used to analyze the PTCH gene mutations in 12 OKCs, including 10 sporadic and 2 nevoid basal cell carcinoma syndrome (NBCCS) associated OKC.
目的分析不同类型地中海贫血（地贫）胎儿基因型与血象各指标特征的关系，探讨血象指标在筛查胎儿地贫中的价值。
Objectives To investigate the relationship between the genotype and the hematologic characteristics in the fetuses with different types of thalassemia.
目的分析不同类型地中海贫血（地贫）胎儿基因型与血象各指标特征的关系，探讨血象指标在筛查胎儿地贫中的价值。
Objectives To investigate the relationship between the genotype and the hematologic characteristics in the fetuses with different types of thalassemia.
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