Ambry Genetics
Project ID
29411
Facility Name
Ambry Genetics
Analyte
PHOX2B full gene mutation analysis in Congenital Central Hypoventilation syndrome (CCHS)
Method
PCR & Sequencing
Specimen Type
saliva; whole blood; chorionic villus sample (CVS); other: cultured amniocytes; other: cultured CVS
Permit Category
Genetic Testing - Molecular
Status
Approved
Facility State
CA
Facility ID
9840