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

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