ArticleClinical genetics2025
A Novel De Novo Missense Variant in Netrin-1 (NTN1) Associated With Chorioretinal Coloboma, Sensorineural Hearing Loss and Polydactyly.
Maria Toms et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
ArticleClinical genetics2025
Maria Toms et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.