Detection of deletions and/or duplications in genes ALX4, MSX2 and RUNX2 by MLPA

Consult

Documentation:
Ref: LV3046 Categories: , , , , , , , Diseases: Cleidocranial dysplasia and isolated cranial ossification defects group: Cleidocranial dysplasia, Parietal foraminaGenes: ALX4, MSX2, RUNX2Delivery term: 28 days