FIGURE
Fig. S3
- ID
- ZDB-FIG-220414-33
- Publication
- Harel et al., 2020 - Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies
- Other Figures
- All Figure Page
- Back to All Figure Page
Fig. S3
ZFIN is incorporating published figure images and captions as part of an ongoing project. Figures from some publications have not yet been curated, or are not available for display because of copyright restrictions. |
Expression Data
| Gene: | |
|---|---|
| Fish: | |
| Anatomical Terms: | |
| Stage Range: | 4-cell to Protruding-mouth |
Expression Detail
Antibody Labeling
Phenotype Data
Phenotype Detail
Acknowledgments