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Reliable diagnostic services
新生兒
緊急新生兒疾病檢測 在疑似有嚴重遺傳疾病的新生兒中, 建立病因診斷是很困難的，因為： 病徵通常是不完整地表現出來。 合併症很常見，包括早產，出生創傷和敗血症等，使臨床表現模糊不清。 兒童疾病進展迅速，導致分秒必爭地確診病因…
自閉症/注意力缺陷過動症
在兩個月內獲得診斷，無需等待多年! 為什麼基因檢測對我懷疑患有自閉症的孩子有用？早期診斷和早期治療的好處…
小兒1000
小兒1000 在兩個月內獲得診斷，無需等待多年 基於多重基因組學技術的基因檢測，包括： 全基因組測序、微陣列芯片、轉錄組等技術，以提高受罕見疾病、發育和神經疾病影響的患者的診斷成功率。
產前檢測
隱性遺傳病攜帶者
產前檢測
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Clinical Trial Design Best Practices
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Clinical Trial Design Best Practices
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Pricing & Plans
Convenient pricing packages
Basic Health Checkup
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$120.00/ Person
- Complete Blood Count
- Glucose Random
- C Reactibe Protein (CRP)
- Lactate Dehydrogenase
- Vitamin D3
Advanced Health Checkup
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$159.00/ Person
- Complete Blood Count
- Glucose Random
- C Reactibe Protein (CRP)
- Lactate Dehydrogenase
- Vitamin D3
career opportunities Future Scope
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- 2018 年 12 月 18 日
- By b950159
Rainbow Genomics 贊助香港醫學遺傳學會第 19 屆年會暨科學會議的外顯子組和藥物基因組學研討會
