PedAM
Pediatric Disease Annotations & Medicines
| Disease | rett syndrome |
| Phenotype | C0003635|apraxia |
| Sentences | 1 |
| PubMedID- 22928142 | A karyotype analysis and molecular testing for angelman syndrome, rett syndrome, and ataxia with oculomotor apraxia type 2 were unrevealing. |
Page: 1