Congenital Central Hypoventilation Syndromes (NextGen Sequencing Panel and Copy Number Analysis; 7 genes)

Clinical Research Prenatal Carrier

Test Details
Disorder◦ Congenital Central Hypoventilation Syndrome
Type◦ Molecular
◦ Multi-Gene Panel
◦ Multi-Method Panel
Method◦ Del/Dup (CNV)
◦ Sequencing, Next Gen
GenesASCL1, BDNF, EDN3, GDNF, HOXA1, PHOX2B, RET
Ordering
Test CodeNGS371
Test URLhttp://mnglabs.com/tests/
Turnaround Time2-4 weeks
ShippingAcceptable specimen types: (1) Blood specimens: Draw blood in an EDTA tube. Preferred volume: 4 milliliters (adults and pediatrics), Minimum volume: 2 milliliters; (2) DNA extracted from leukocytes, muscle, or fibroblasts: Preferred quantity: 4 micrograms, Minimum quantity: 3 micrograms (Genomic DNA should be eluted in sterile Dnase/Rnase free water or TE. The A260:A280 ratio should be 1.8-2.0.); (3) 2 T-25 flasks of fibroblasts; (4) 50-75 milligrams muscle snap frozen in liquid nitrogen and maintained at -80
Billing
Billing InfoPlease see https://mnglabs.com/providers/billing-information/ for billing information
CPT Code81479
 

Laboratory

MNG Laboratories (Medical Neurogenetics, LLC.)
5424 Glenridge Dr. NE
Atlanta
GA 30342
USA

email: quickresponse@mnglabs.com

Lab Details

 

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