Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Chromosome Anomaly, Deletion, 22q11.2

IVD Test Reagent/Kits, Molecular Assay, Chromosome Anomaly, Deletion, 22q11.2

Definition : Molecular assay reagents intended for use in identifying deletions in chromosome 22 band q11.2. These genetic deletions are present in patients with an inherited autosomal dominant disorder characterized by congenital heart disease (in 3/4 of individuals), velopharyngeal incompetence, cleft palate, learning difficulties, and immunodeficiency.

Entry Terms : "Autosomal Dominant Opitz Syndrome Diagnostic Reagents" , "Cayler Cardiofacial Syndrome Diagnostic Reagents" , "Conotruncal Anomaly Face Syndrome (CTAF) Diagnostic Reagents" , "Shprintzen Syndrome Diagnostic Reagents" , "Velocardiofacial Syndrome (VCFS) Diagnostic Reagents" , "Di George Syndrome (DGS) Diagnostic Reagents" , "22q11.2 Deletion Syndrome Diagnostic Reagents" , "Tumor Markers" , "Reagents, Molecular Assay, Chromosome Anomaly, Deletion, 22q11.2"

UMDC code : 24078

Filters
Manufacturers
Distributors
U.S.companies only
Suppress Subsidiary Companies
   

No results at this time.

 

Medical Product Guide Ophthalmology Management Product Guide