Associated Papers
A Rare Craniosynostosis Phenotype Associated With a Homozygous CYP26B1 Pathogenic Variant in the Absence of Extremity Synostosis.
Caliskan BO et al.
American Journal of Medical Genetics. Part A, 2026
CYP26B1-related disorder: expanding the ends of the spectrum through clinical and molecular evidence.
Silveira KC et al.
Human Genetics, 2023
Familial monoallelic CYP26B1 truncating variant causes a syndromic craniosynostosis due to haploinsufficiency ?
Sarma AS et al.
European Journal of Medical Genetics, 2023
Nonlethal presentations of CYP26B1-related skeletal anomalies and multiple synostoses syndrome.
Grand K et al.
American Journal of Medical Genetics. Part A, 2021
Frequent FOXA1-Activating Mutations in Extramammary Paget's Disease.
Takeichi T et al.
Cancers, 2020
32235312 (PubMed )
Supplement: cancers-12-00820-s001.pdf
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