nstd202 (Ghazali et al. 2021)
- Organism:
- Human
- Study Type:
- Somatic
- Submitter:
- Norliana Ghazali
- Description:
- This study identified the genetic aberration involved in both NSCL/P and hypodontia pathogenesis. There were a significant gain and loss, of both SKI and FHIT copy number in NSCL/P with hypodontia compared to the non-cleft group (p<0.05). The results supported that CNVs significantly furnish to the development of NSCL/P with hypodontia. See Variant Summary counts for nstd202 in dbVar Variant Summary.
- Publication(s):
- Ghazali et al. 2021