Beckwith-Wiedemann Syndrome
| TEST CODE | MG04050 |
| TEST NAME | Beckwith-Wiedemann Syndrome |
| RELATED GENE | CDKN1C |
| SYNONYMOUS | CDKN1C |
| OMIM | 130650 |
| HEREDITY | Autosomal Dominant |
| CLINICAL AREA | Beckwith – Wiedemann Syndrome is an autosomal dominantly inherited disease. Mutations in the CDKN1C gene have been associated with the disease. |
| METHOD | Next Generation Sequencing |
| SAMPLE TYPE | Heparinized Blood |
| QUANTITY | 3 mL |
| TAT | 15 DAYS |
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