McCammon et al., 2017
- The 16p11.2 homologs fam57ba and doc2a generate certain brain and body phenotypes.
Human molecular genetics
26:3699-3712
Full text @ Hum. Mol. Genet.
Human Disease | Fish | Environment | Evidence Code |
---|---|---|---|
autistic disorder | |||
chromosome 16p11.2 deletion syndrome, 220-kb |