Fanconi Anemia Panel (18 Genes)
| TEST CODE | MGQ0010 |
| TEST NAME | Fanconi Anemia Panel (18 Genes) |
| RELATED GENE | BRCA2, BRIP1, ERCC4, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, RAD51C, SLX4, UBE2T, XRCC2 |
| SYNONYMOUS | BRCA2, BRIP1, ERCC4, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, RAD51C, SLX4, UBE2T, XRCC2 |
| OMIM | |
| HEREDITY | |
| CLINICAL AREA | Fanconi Anemia (FA) is a rare hereditary chromosome breakage syndrome characterized by physical abnormalities, bone marrow failure, and increased risk of various malignancies. Many different genes, mostly involved in DNA repair, constitute the genetic infrastructure of FA. Within the scope of the panel, 18 genes associated with Fanconi anemia are examined. |
| METHOD | Next Generation Sequencing (NGS) |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 mL |
| TAT | 21 DAYS |
ORDER OPTIONS AND PRICING
Discover genetic insights at your convenience. Contact Mikrogen anytime for information on order options, pricing, and comprehensive genetic testing services