Associated Papers
Currarino syndrome: a comprehensive genetic review of a rare congenital disorder.
Dworschak GC et al.
Orphanet Journal of Rare Diseases, 2021
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis.
Boissel S et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2018
Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation.
Crétolle C et al.
Human Mutation, 2008
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