Associated Papers
Molecular landscape of congenital vertebral malformations: recent discoveries and future directions.
Szoszkiewicz A et al.
Orphanet Journal of Rare Diseases, 2024
Currarino syndrome: a comprehensive genetic review of a rare congenital disorder.
Dworschak GC et al.
Orphanet Journal of Rare Diseases, 2021
Novel MNX1 mutations and genotype-phenotype analysis of patients with Currarino syndrome.
Han L et al.
Orphanet Journal of Rare Diseases, 2020
Select a paper to view details