Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.
The record is no longer available at this source.
Proper Citation: RRID:MGI:3053579
Description: Allele Detail: Targeted This is a legacy resource.
Species: Mus musculus
Notes: Allele Detail: Targeted This is a legacy resource.
Phenotype: abnormal sphenoid bone morphology, ocular hypertelorism, decreased molar number, domed cranium, increased osteoblast cell number, exophthalmos, premature coronal suture closure, abnormal frontal bone morphology, premature cranial suture closure, short face, short maxilla, premature coronal suture closure, malocclusion
Affected Gene: Fgfr2
Expand AllWe found {{ ctrl2.mentions.all_count }} mentions in open access literature.
We have not found any literature mentions for this resource.
We are searching literature mentions for this resource.
Most recent articles:
{{ mention._source.dc.creators[0].familyName }} {{ mention._source.dc.creators[0].initials }}, et al. ({{ mention._source.dc.publicationYear }}) {{ mention._source.dc.title }} {{ mention._source.dc.publishers[0].name }}, {{ mention._source.dc.publishers[0].volume }}({{ mention._source.dc.publishers[0].issue }}), {{ mention._source.dc.publishers[0].pagination }}. (PMID:{{ mention._id.replace('PMID:', '') }})
A list of researchers who have used the resource and an author search tool
A list of researchers who have used the resource and an author search tool. This is available for resources that have literature mentions.
No rating or validation information has been found for Fgfr2tm4Lni/Fgfr2+.
No alerts have been found for Fgfr2tm4Lni/Fgfr2+.
Source: Integrated Animals
Source Database: MGI, Mouse Genome Informatics MGI