Associated Papers
A Heterozygous Novel Mutation in TFAP2A Gene Causes Atypical Branchio-Oculo-Facial Syndrome With Isolated Coloboma of Choroid: A Case Report.
Min J et al.
Frontiers in Pediatrics, 2020
Branchio-oculo-facial syndrome in a newborn caused by a novel TFAP2A mutation.
Günes N et al.
Genetic Counseling (geneva, Switzerland), 2014
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