The way we measure
Procedure |
---|
Combined SHIRPA and Dysmorphology |
Phenotype associations stats
0.00% of tested genes with null mutations on a B6N genetic background have a phenotype association to malocclusion (0/1113)
0.00% females (0/1114) 0.00% males (0/1113)
The IMPC Newsletter
Get highlights of the most important data releases, news and events, delivered straight to your email inbox
Subscribe to newsletter