Craniofrontonasal Dysplasia

TEST CODE MG04170
TEST NAME Craniofrontonasal Dysplasia
RELATED GENE EFNB1
SYNONYMOUS EFNB1
OMIM 304110
HEREDITY X-Linked Dominant
CLINICAL AREA Craniofrontonasal Dysplasia is an X-linked dominantly inherited disease. Mutations in the EFNB1 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