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Reagents, Molecular Assay, Chromosome Anomaly, Deletion, 15q11.2-q13

Definition : Molecular assay reagents intended for use in identifying deletions in the Angelman syndrome/Prader-Willi syndrome (AS/PWS) region, located in 15q11.2-q13. This genetic deletion is the most frequent and severe genetic abnormality in patients with Prader-Willi syndrome.

Entry Terms : "Prader-Willi Syndrome/Angelman Syndrome (PWS/AS) Diagnostic Reagents" , "Angelman Syndrome/Prader-Willi Syndrome (AS/PWS) Diagnostic Reagents" , "Prader-Willi Syndrome (PWS) Diagnostic Reagents"

UMDC code : 24080

   

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