P366: MED13 associated with multiple congenital anomalies and a Goldenhar syndrome phenotype
Fields of Study & Subjects
Craniofacial Disorders and Treatments
Genomics and Rare Diseases
Congenital Ear and Nasal Anomalies
Publication details
- Journal / source
- Genetics in Medicine Open
- Volume
- 4
- Pages
- 103860–103860
- Publication date
- 1 January 2026
- Language
- EN