FIGURE
Fig. S3
- ID
- ZDB-FIG-130826-1
- Publication
- Arndt et al., 2013 - Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy
- 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: | Prim-5 to Protruding-mouth |
Expression Detail
Antibody Labeling
Phenotype Data
Phenotype Detail
Acknowledgments