HOXA2 - microtia, hearing impairment, and cleft palate
This test is available for the following conditions:
- Conditions > Multiple congenital anomalies (MCA) > Microtia, hearing impairment, and cleft palate
- Conditions > Hearing impairment > Microtia, hearing impairment, and cleft palate
This product is also part of the following panels:
- Comprehensive preconception carrier test panel¹
- Craniofacial anomalies panel with genome wide CNV analysis
- Mendelian inherited disorders panel with genome wide CNV analysis
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
604685
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane