Associated Papers
Two novel compound heterozygous HOXB1 variants in congenital facial palsy: A case report and a brief review of the literature.
Brugnoli C et al.
American Journal of Medical Genetics. Part A, 2025
A framework for the evaluation of patients with congenital facial weakness.
Webb BD et al.
Orphanet Journal of Rare Diseases, 2021
A Novel Loss-of-Function Mutation in HOXB1 Associated with Autosomal Recessive Hereditary Congenital Facial Palsy in a Large Iranian Family.
Vahidi Mehrjardi MY et al.
Molecular Syndromology, 2017
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