Molecular Diagnostics & DNA Testing
DNA Labs India | Diagnostic Tests
Molecular Diagnostics & DNA Testing
Clinical Overview
Sub-category mapping under Pediatrics & Neonatology
| Reviewed by: Dr. Rajesh Kumar, MD Pathology | ISO 9001:2015 Certified Laboratory
This content is for educational purposes only. Always consult a qualified healthcare provider for medical advice.
Tests
ZIC1 Gene Craniosynostosis type 6 NGS Genetic Test
The purpose of the ZIC1 Gene Craniosynostosis Type 6 NGS Genetic Test is to accurately diagnose Cran...
FGFR2 Gene Crouzon syndrome NGS Genetic Test
To diagnose Crouzon syndrome by detecting pathogenic mutations in the FGFR2 gene using NGS technolog...
CENPE Gene Microcephaly, autosomal recessive type 13 NGS Genetic Test
The purpose of this test is to identify mutations in the CENPE gene that cause autosomal recessive m...
ASPM Gene Microcephaly, autosomal recessive type 5 NGS Genetic Test
To identify mutations in the ASPM gene for definitive diagnosis of autosomal recessive microcephaly...
AGPS Gene Rhizomelic chondrodysplasia punctata type 3 NGS Genetic Test
The purpose of the AGPS Gene Rhizomelic chondrodysplasia punctata type 3 NGS Genetic Test is to diag...
WASHC5 Gene Ritscher-Schinzel syndrome type 1 NGS Genetic Test
To identify mutations in the WASHC5 gene that cause Ritscher-Schinzel Syndrome Type 1, aiding in dia...
chr. 11p15 Gene Silver-Russell syndrome NGS Genetic Test
The purpose of this test is to identify genetic mutations in the chr. 11p15 gene that cause Silver-R...
TWIST1 Gene Craniosynostosis type 1 NGS Genetic Test
To identify mutations in the TWIST1 gene for diagnosis of craniosynostosis type 1, aiding in early i...
FLVCR2 Gene Hydranencephaly, Fowler type NGS Genetic Test
To identify mutations in the FLVCR2 gene that cause hydranencephaly, Fowler type, aiding in diagnosi...