Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Chromosome Anomaly, Trisomy, Congenital

IVD Test Reagent/Kits, Molecular Assay, Chromosome Anomaly, Trisomy, Congenital

Definition : Molecular assay reagents intended for use in identifying the inborn (i.e., congenital) presence of three chromosomes in a patient sample (e.g., fetal cells from amniotic fluid), rather than the normal two (i.e., trisomy). Congenital trisomies are typically characterized by physical and developmental disorders. The most common congenital trisomies occur in chromosome 21 (i.e., Down syndrome), chromosome 18 (i.e., Edwards' syndrome), and chromosome 13 (i.e., Patau's syndrome); but trisomies may occur in other chromosomes (e.g., 8, 11, 22).

Entry Terms : "Molecular Assay Reagents, Inborn Disorder" , "Congenital Trisomy Detection Reagents" , "Reagents, Molecular Assay, Inborn Disorder, Chromosomal, Trisomy" , "IVD Test Reagent/Kits, Molecular Assay, Inborn Disorder, Chromosomal" , "IVD Test Reagent/Kits, Molecular Assay, Inborn Disorder" , "Trisomy Determination Reagents" , "Inborn Disorder Determination Reagents, Chromosomal" , "Chromosomal Inborn Disorder Determination Reagents" , "Reagents, Molecular Assay, Chromosome Anomaly, Trisomy, Congenital"

UMDC code : 19610

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PerkinElmer Inc

Company Type: Parent

As a global technology leader, PerkinElmer is taking action to harness the power of insights and transform them into knowledge to deliver innovative, differentiated solutions for our customers. From critical therapeutic and disease research and prenatal screening, to environmental testing and industrial monitoring, we are actively engaged in improving health and advancing quality and longevity of life all around the world.

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