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        Personalized Carrier Screening Test
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        PGT-M with NGS for monogenic diseases
        – most frequent mutations
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        PGT with NGS for X-linked diseases
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Hotline:

+48 696 059 658

info@invictagenetics.com

INVICTA Genetics Laboratory
  • About us
    • Overview
    • Our team
    • Quality
    • News
    • Upcoming events
  • Services
    • Preconception Genetic Testing
      • FertiGenes Test™
        Fertility and RPL Genetic Testing
      • BRCA 1/2 Test™
        Full genes sequencing – NGS
      • CFTR Test™
        Carrier Testing for Cystic Fibrosis
      • Open Frame™
        Personalized Carrier Screening Test
      • Chromosome Analysis
        Karyotype (G-banding)
      • Counseling
        Genetic Counseling
    • Preimplantation Genetic Testing (PGT)
      • PGDA NGS 360°™
        PGT-A with NGS for aneuploidy screening
      • PGD TRS™
        PGT-SR with NGS for structural rearrangements
      • PGD ONE FM™
        PGT-M with NGS for monogenic diseases
        – most frequent mutations
      • PGD X-Linked™
        PGT with NGS for X-linked diseases
    • Recurrent Pregnancy Loss (RPL)
      • iMGE Test™
        Product of Conception
      • FertiGenes Test™
        Recurrent Pregnancy Loss Test
      • Chromosome Analysis
        Karyotype (G-banding)
  • Test information
    • Shipping Information
    • Shipping kits
    • Sample Taking Instructions
    • Referral note and Consent Forms
    • The process and documents needed for the PGT service
  • PUBLICATIONS
  • Contact

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INVICTA GENETICS
ul. Polna 64, 81-740
Sopot, Poland
Customer Service
+48 58 58 58 800
E-mail: info@invictagenetics.com
  • About us
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