Preimplantation genetic testing for mutations in embryos using Sanger sequencing and STR analysis…. This lab test includes home sample collection via a provided kit or by a clinician, and you’ll receive a comprehensive physical health report with your results.
PGT-M for common and rare disease by Direct Sequencing (add on embryo)
19,800 THB
SKU :
MD-NLMM125
Preimplantation genetic testing for mutations in embryos using Sanger sequencing and STR analysis.
Lab Categories : Adults, EDTA Whole Blood, Embryos, Family Planning, Genetic Disorders, Lab Test, N/A, Sanger Sequencing, STR Analysis
Tags : Family Planning, Genetic Disorders, N/A, PGT-M for Embryos
Diseases : Genetic Disorders
Symptoms : N/A
Habits : Family Planning
Age Groups : Adults
Specimens : EDTA Whole Blood, Embryos
Diagnostic Methods : Sanger Sequencing, STR Analysis
| Also Known As | PGT-M for Embryos |
|---|---|
| Specimen | – EDTA whole blood >= 3 mL. – EDTA whole blood >= 3 mL. – Embryos: Cleavage Stage Day 3 or Blastocyst Day 5 or Day 6 * Genotype |
| Turnaround Time | 3 months |
| Test Code | MD-NLMM125 |
| Test Type | Special |
| Related Tests | Genetic Testing |
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