We're Moving to
The content you are trying to access has moved to new site. Explore, discover (and in certain contries, buy) our products and services on our new website. Click to visit now or you will be automatically redirected.
to view non-migrated solutions
PerkinElmer科学家已经与威尔士大学医院和卡迪夫大学的科研人员合作，共同开发了一款针对杜氏肌营养不良症的新型免疫分析筛查测试。
菲律宾正在庆祝新生儿筛查二十周年，宣布将进一步扩大该计划及其目标。
A fully automated high throughput batch analyzer for quantitative or qualitative measurement of neonatal screening samples on 96-well microplates.
Quantitative determination of TREC (T-cell receptor excision circle) DNA as an aid in screening newborns for severe combined immunodeficiency (SCID).
TQD (Tandem Quadrupole Detector) represents the latest MSMS instrumentation for newborn screening applications.
新生儿的特定遗传缺陷，虽然比较罕见，但是如果没有被发现，可能会危害健康甚至危及生命。及早检测代谢和其他遗传疾病可帮助改善儿童及其家庭的生活。
仅通过出生时采集的针刺足跟血样，我们的仪器或我们在美国的服务实验室就可提供超过 50 种缺陷的筛查测试。