Associated Papers
CDON Mutation Related to Nose Deformity with Variable Expression in Holoprosencephaly in an Iranian Family: A Case Report.
Farhud DD et al.
Iranian Journal of Public Health, 2024
CDON gene contributes to pituitary stalk interruption syndrome associated with unilateral facial and abducens nerve palsy.
Obara-Moszyńska M et al.
Journal of Applied Genetics, 2021
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