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 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
A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis.
Sahin Y et al.
Brain & Development, 2017
Homozygous HOXB1 loss-of-function mutation in a large family with hereditary congenital facial paresis.
Vogel M et al.
American Journal of Medical Genetics. Part A, 2016
A new hereditary congenital facial palsy case supports arg5 in HOX-DNA binding domain as possible hot spot for mutations.
Uyguner ZO et al.
European Journal of Medical Genetics, 0
Select a paper to view details