Associated Papers
Spectrum of MNX1 Pathogenic Variants and Associated Clinical Features in Korean Patients with Currarino Syndrome.
Lee S et al.
Annals of Laboratory Medicine, 2018
Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation.
Crétolle C et al.
Human Mutation, 2008
Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome.
Garcia-Barceló M et al.
Clinical Chemistry, 2006
Select a paper to view details