Associated Papers
Evaluation of Sporadic and Familial Cases with Craniofrontonasal Syndrome: A Wide Clinical Spectrum and Identification of a Novel EFNB1 Gene Mutation.
Gürsoy S et al.
Molecular Syndromology, 2021
Extracranial midline defects in a patient with craniofrontonasal syndrome with a novel EFNB1 mutation.
Acosta-Fernández E et al.
American Journal of Medical Genetics. Part A, 2020
Additional EFNB1 mutations in craniofrontonasal syndrome.
Wallis D et al.
American Journal of Medical Genetics. Part A, 2008
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