A Rare Craniosynostosis Phenotype Associated With a Homozygous CYP26B1 Pathogenic Variant in the Absence of Extremity Synostosis
Year: 2025
Type: article
Study design: Case Report
DOI: 10.1002/ajmg.a.64257
Authors: Busra Ozguc Caliskan, Mikail Demir, Suat Oktem, Selcan Ozturk, Mehmet Canpolat, Munis Dundar
Institution: Erciyes University
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W4414555124