Trisomy 21, 18, 13, Tunners Syndrome (XO), Triple X Syndrome (XXX),Klinefelter’s Syndrome (XXY), Jacob’s Syndrome (XYY), Chromosomal Deletions (DiGeorge Syndrome), Other Autosomal Aneuploidies, (1,2,3,4,5,6,7,8,9,10,11,12,14,15,16,17,18,19,20,22), 25 Dominant Single Gene Disorder, Carrier Screening for 9 COMMON GENETIC,DISEASE (Alpha Thalassemia, Beta Thalassemia, Galactosemia, Phenylketonuria, G6PD, Deficiency, Citrin Deficiency, Steroid 5 alpha- reductase 2 Deficiency, Glycogen Storage Disease
By: QUIRINO MEMORIAL MEDICAL CENTER📍 PhilippinesClosed
Key Information
| Reference | GB-90284 |
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| Deadline | Oct 5, 2026 12:00 AM |
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| Category | Advertising & Media |
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| Competition Type | ICB |
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| Funding Source | Self-Funded |
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| Country | Philippines |
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| Address | Philippines |
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| Published | Oct 2, 2026 |
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Description
Trisomy 21, 18, 13, Tunners Syndrome (XO), Triple X Syndrome (XXX),Klinefelter’s Syndrome (XXY), Jacob’s Syndrome (XYY), Chromosomal Deletions (DiGeorge Syndrome), Other Autosomal Aneuploidies, (1,2,3...
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