Associated Papers
Genetic Mutations in Cell Junction Proteins Associated with Brain Calcification.
Yang D et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2025
Phenotypic and mutational spectrum of ROR2-related Robinow syndrome.
Lima AR et al.
Human Mutation, 2022
Sclerosteosis: Report of type 1 or 2 in three Indian Tamil families and literature review.
Whyte MP et al.
Bone, 2018
A review on non-syndromic tooth agenesis associated with PAX9 mutations.
Fauzi NH et al.
The Japanese Dental Science Review, 2018
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