Name ID |
D2.129S6(Cg)-Fgfr1tm2.1Cxd MGI:5790246 |
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Mouse Phenotypes | abnormal basisphenoid bone morphology |
abnormal maxillary-premaxillary suture morphology |
abnormal palatine bone morphology |
abnormal viscerocranium morphology |
midface hypoplasia |
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Availability | Mouse Genotype | |||||
Fgfr1tm2.1Cxd/Fgfr1+ |