Apert Syndrome
| TEST CODE | MG00570 |
| TEST NAME | Apert Syndrome |
| RELATED GENE | FGFR2 |
| SYNONYMOUS | FGFR2 |
| OMIM | 101200 |
| HEREDITY | Autosomal Dominant |
| CLINICAL AREA | Apert Syndrome is a disease inherited as Autosomal Dominant. Mutations in the FGFR2 gene have been associated with the disease. |
| METHOD | Next Generation Sequencing |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 ml |
| TAT | 40 DAYS |
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