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  • About us
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  • Patients
    • Embryo
      • Embryo biopsy
      • PGD of monogenic diseases
      • Chromosomal PGD
    • Pregnancy
      • Rapid prenatal diagnosis
      • Prenatal chromosomal diagnosis CGH arrays
      • Prenatal diagnosis of monogenic diseases
      • Chromosomal analysis in spontaneous abortions
    • Adults and children
    • How to access our services
  • Specialists
    • Preimplantational diagnosis
      • Embryo biopsy
      • Informative study in carriers of structural anomalies
      • PGD in carriers of structural anomalies
      • PGD in 5 or 9 cromosomal aneuploidies by fish
      • PGD in 24 cromosomal aneuploidies by CGH array
      • PGD of monogenic diseases
      • Chromosomal PGD
    • Prenatal diagnosis
      • Prenatal diagnosis
      • Rapid prenatal diagnosis by QF-PCR
      • Rapid prenatal diagnosis by means of BoBs
      • CGH Array
      • Prenatal diagnosis of monogenic diseases
      • Chromosomal analyses in spontaneous abortions
    • Genetic diagnosis in adults and postnatal
      • ERA
      • GIC
      • 5-Chromosome spermatozoid FISH
      • Reproductive genomics
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Copyright 2012
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The NACE Plus test is designed to rule out the presence of the most frequent chromosomal alterations in single pregnancies without putting the pregnancy at risk.

It is especially suitable for women with a high risk of chromosomal abnormalities after screening in the 1st trimester*, with previous Down syndrome pregnancies or where suspicious alterations have been detected in scans.

Given the characteristics and safety of the test, it can be used by women of any age in the following situations:

Where there has been test-tube fertilisation and, particularly, for pregnancies using donated ova.

Independent of body mass or ethnic group.
Site Map | Contact | legal
Mapa del web | Contacto | Nota legal
Site Map | Contact | Legal