Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and mice

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Figure 3.
Figure 3.

Expression of Zak in mouse embryos. In situ hybridization using a probe for Zak on mouse embryos at the indicated embryonic days. (Top) Whole embryos; (bottom) magnifications of the forelimb (FL).

This Article

  1. Published in Advance January 11, 2016, doi: 10.1101/gr.199430.115 Genome Res. 26: 183-191

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