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Phenotype: P0 pronuclear meeting position abnormal
| P0 pronuclear meeting position abnormal | Description | Position near the cortex or centrally (wild type: near the centre of the posterior half of the embryo) | |
|---|---|---|---|
| Assay | visual inspection | ||
| Related_phenotypes | Specialisation_of | Emb | |
| embryonic defect | |||
| Attribute (2) |
