The Common carrier screening panel is designed to detect carriers of disorders commonly tested by carrier screening. These disorders are severe, childhood onset disorders with autosomal recessive or X-linked inheritance that have been recommended or suggested by the American College of Obstetrics and Gynecology (ACOG) or the American College of Genetics and Genomics (ACMG) for inclusion on carrier screening panels.read more
18 Panel Genes: ASPA, BCKDHA, BLM, CFTR, DMD, ELP1, FANCC, FMR1, GBA, HBA1, HBA2, HBB, HEXA, MCOLN1, PAH, SMN1, SMN2, SMPD1
Next Gen Sequencing & Del/Dup Analysis PCR Fragment Length Analysis
Test Code: 6000
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Typically within 2 weeks from receipt of a sample in the laboratory.
1. Whole blood: purple-top (EDTA) tube, minimum of 3 ml
2. Genomic DNA: a minimum of 3 ug (at a concentration of at least 30 ng/ul)
Ship all specimen types at room temperature by overnight courier. Do not freeze.