Cleidocranial Dysostosis
TEST CODE | MG08890 |
TEST NAME | Cleidocranial Dysostosis |
RELATED GENE | RUNX2 |
SYNONYMOUS | RUNX2 |
OMIM | 600211 |
HEREDITY | Autosomal Dominant |
CLINICAL AREA | Cleidocranial Dysostosis is an autosomal dominantly inherited disease. Mutations in the RUNX2 gene have been associated with the disease. |
METHOD | Next Generation Sequencing |
SAMPLE TYPE | Blood with EDTA |
QUANTITY | 3 ml |
TAT | 40 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