Comprehensive Genetic & Molecular Diagnostic Services
Explore our comprehensive diagnostic offerings, combining precision technology with compassionate patient care.
🧬 In-House Genetic Screening & Prenatal Diagnosis
Accurately identify inherited disorders
Services include:
- Thalassemia screening & prenatal diagnosis
- Hemophilia genetic testing
- Down Syndrome screening
- Duchenne Muscular Dystrophy (DMD)
- Carrier screening for inherited disorders
✔ Fast turnaround
✔ Local testing & expert reporting
✔ Confidential & reliable results
🧬 Advanced Genomic Testing
Authorized Collaboration with Macrogen (South Korea) and BGI (Hong Kong)
Advanced NGS-based genomic testing through our authorized partnership with Macrogen.
- Whole Exome Sequencing (WES)
- Whole Genome Sequencing (WGS)
- Targeted mutation & gene panel analysis
✔ Global expertise
✔ Advanced bioinformatics analysis
✔ Clinically actionable reports
🧪 Non-Invasive Prenatal Testing (NIPT)
In Collaboration with BGI
Our NIPT service uses advanced NGS technology to screen fetal chromosomal abnormalities from a simple maternal blood sample.
Discover Our Specialized Services
Highlighting advanced prenatal and diagnostic testing expertise.
Our Expertise – Prenatal Genetic Testing
Prenatal genetic testing is a powerful tool that allows parents to understand the health of their baby before birth. Through advanced molecular techniques, we can detect genetic abnormalities and inherited disorders during pregnancy.
We Specialize In Prenatal Diagnosis:
- Thalassemia
- Hemophilia
- Trisomy 21 Down syndrome, 18 Edwards syndrome , 13 Patau syndrome
- Duchenne muscular dystrophy (DMD)
- SMA (Spinal Muscular Atrophy)
- Other Complex genetic disorders of unknown Etiology (By Whole Genome/Whole Exome/Gene Panels analysis)
Expertise with Over a Decade of Experience
Trustworthy diagnostics backed by years of professional practice.
Contact Us
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