Xla Wt + cyp26a1 + aldh1a2 MO has 1 phenotype(s)
Images Sources Experiment + Assay Phenotypes Human Diseases
Fig.5.B,E

Gur M et al. (2022)
Xla Wt + cyp26a1 + aldh1a2 MO

NF32 (whole-mount microscopy)
Anatomical Phenotype
abnormal development of eye
decreased size of the head
microcephaly