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
Compound heterozygous splicing CDON variants result in isolated ocular coloboma.
Reis LM et al.
Clinical Genetics, 2020
Exome sequencing in patients with microphthalmia, anophthalmia, and coloboma (MAC) from a consanguineous population.
Islam F et al.
Clinical Genetics, 2020
Homozygous variants in MAPRE2 and CDON in individual with skin folds, growth delay, retinal coloboma, and pyloric stenosis.
Berkun L et al.
American Journal of Medical Genetics. Part A, 2019
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