遗传筛查为妇女提供了一个希望，那就是让她们更好的了解自己患上乳腺癌的几率。
For women, genetic screening offers the hope of better understanding the likelihood that they'll develop breast cancer.
她和她的同事得出结论：考虑到遗传筛查所需费用，现在还不值得在临床上引入。
She and her colleagues conclude that, given the cost involved, genetic screening is not worthwhile in a clinical context.
四项是同龄组研究，也就是说研究开始时对一个健康人群做遗传筛查，然后观测其后的15年他们中哪些人会患上乳腺癌，哪些人不会。
Four were cohort studies in which a healthy population was genetically screened at the outset and followed for 15 years to see who developed breast cancer and who did not.
在有些中心做胚胎植入前遗传诊断(PGD)筛查遗传病。
Preimplantation genetic diagnosis (PGD) is performed at some centers to screen for inherited diseases.
产前筛查是提供对国民保健服务，这可以让你进行一次血液检测承运人夫妇，并提供遗传咨询。
Antenatal screening is offered on the NHS, this allows you to undergo a blood test to detect carrier couples and provide genetic counselling.
PGD适用于特殊遗传病的筛查，如囊性纤维化和神经节苷脂病，而且PGD也可以用于性别选择。
PGD is good for screening for specific genetic disorders such as cystic fibrosis and Tay-Sachs disease, and also can be used to select gender.
而那些不具有危险性遗传标志的男性，无需进行此类筛查。
Men who do not carry genetic markers of risk may not need such screening measures.
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.
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：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.
在这里，我们描述单倍体胚胎干细胞显示他们在正向遗传学筛查中的应用。
Here we describe haploid mouse embryonic stem cells and show their application in forward genetic screening.
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 f...
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 suscept...
美国医学遗传学和基因组学院也建议进行囊性纤维化和肌萎缩症筛查。
The American College of Medical Genetics and Genomics also recommends screening for CF and SMA.
筛查后，由公司在线提供筛查结果，如果后续有问题，客户可以向医生和遗传咨询师进行咨询。
After the company delivers results online, customers can ask physicians and genetic counselors follow up questions.
筛查后，由公司在线提供筛查结果，如果后续有问题，客户可以向医生和遗传咨询师进行咨询。
After the company delivers results online, customers can ask physicians and genetic counselors follow up questions.
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