Congenital Central Hypoventilation Syndrome (PHOX2B)

PHOX2B sequencing and deletion/duplication analysis

Clinical Research Prenatal Carrier

Test Details
Disorder◦ Congenital Central Hypoventilation Syndrome
Type◦ Molecular
◦ Multi-Method Panel
Method◦ Del/Dup (CNV)
◦ Sequencing, Next Gen
GenesPHOX2B
Ordering
Test CodePHOX2B
Test URLhttp://www.geneticscenter.com/services/cancer-panel/
Turnaround Time7-10 days
Preferred SpecimenBlood: A single tube with 1-5 mL whole blood in EDTA (lavender top).
Alternate SpecimenSaliva: Please contact us for collection kit.
ShippingShipping: Store blood at 4C until shipment. Ship at ambient temperature in an insulated container via overnight delivery within 96 hours of collection.
Billing
New York Approved
 

Laboratory

Genetics Center
211 S. Main Street
Orange
CA 92868
USA

email: contact@geneticscenter.com

Lab Details

 

Follow GeneTests

 

Share

Write a comment ...
Post Comment
Cancel