Name ID |
B6.129P2-Fgfr3tm1.1Aomw MGI:3831532 |
Darker colors indicate more annotations |
Mouse Phenotypes | abnormal coronal suture morphology |
abnormal cranial suture morphology |
abnormal cranium morphology |
abnormal foramen magnum morphology |
abnormal lambdoid suture morphology |
abnormal neurocranium morphology |
abnormal occipital bone morphology |
abnormal premaxilla morphology |
decreased cranium height |
enlarged interparietal bone |
malocclusion |
synostosis |
thin frontal bone |
thin parietal bone |
|
Availability | Mouse Genotype | ||||||||||||||
Fgfr3tm1.1Aomw/Fgfr3+ | |||||||||||||||
Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw |