eP263: A pathogenic deletion at 13q32.1q33.1 presenting with bilateral sensorineural hearing loss and pigmentation anomalies, mimicking Waardenburg syndrome
- Resource Type
- Article
- Source
- Genetics in Medicine; March 2022, Vol. 24 Issue: 3, Number 3 Supplement 1 pS166-S167, 2p
- Subject
- Language
- ISSN
- 10983600; 15300366