Clinical and Molecular Analyses in 8 New Craniofrontonasal Syndrome Families: Revisiting the Mild End of the Phenotypic Spectrum in Females

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dc.contributor.authorAltunoglu, Umut
dc.contributor.authorKaraman, Birsen
dc.contributor.authorAlanay, Yasemin
dc.contributor.authorPercin, Ferda
dc.contributor.authorUyguner, Zehra Oya
dc.contributor.authorKayserili, Huelya
dc.date.accessioned2025-10-16T15:11:59Z
dc.date.issued2025
dc.identifier.doi10.5152/TurkArchPediatr.2025.24336
dc.identifier.otherWOS:001451396100011
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/5170
dc.publisherAVES
dc.sourceTURKISH ARCHIVES OF PEDIATRICS
dc.subjectCraniofrontonasal syndrome
dc.subjectEFNB1
dc.subjectclinical paradox
dc.subjectmild female phenotype
dc.titleClinical and Molecular Analyses in 8 New Craniofrontonasal Syndrome Families: Revisiting the Mild End of the Phenotypic Spectrum in Females
dc.typeArticle

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