FIGURE SUMMARY
Title

Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies

Authors
Harel, T., Griffin, J.N., Arbogast, T., Monroe, T.O., Palombo, F., Martinelli, M., Seri, M., Pippucci, T., Elpeleg, O., Katsanis, N.
Source
Full text @ Hum. Mol. Genet.
Fig. 2

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.

Fig. 3

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.

Fig. 4

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.

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 / LABELING:
Gene:
Fish:
Anatomical Terms:
Stage Range: 4-cell to Protruding-mouth
Acknowledgments
Full text @ Hum. Mol. Genet.
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