Congenital Central Hypoventilation Syndrome (PHOX2B sequence analysis)

Sequencing, Capillary

Clinical Research Prenatal Carrier

Test Details
Disorder◦ Congenital Central Hypoventilation Syndrome
Type◦ Molecular
Method◦ Sequencing, Capillary (Sanger)
GenesPHOX2B
Locus4p13
Ordering
Test URLhttp://apps.chop.edu/service/laboratories/olsd.cfm/laboratories/AE7C807B-1C25-1479-5592924C704C7544
Turnaround Time4-6 weeks
Preferred Specimen3-5 mL whole blood in EDTA (lavender top tube)
ShippingShip overnight at ambient temperature.
Billing
Billing InfoPlease visit: http://www.chop.edu/service/laboratories/explore-chop-labs/labs-molecular-genetics/forms.html
Current CPT Code81404
New York Approved
ABN Required
 

Laboratory

Children's Hospital of Philadelphia, Division of Genomic Diagnostics
3615 Civic Center Blvd
Philadelphia
PA 19104
USA

email: DGDGeneticCounselor@email.chop.edu

Lab Details

 

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