Associated Papers
POU3F3-related disorder: Defining the phenotype and expanding the molecular spectrum.
Rossi A et al.
Clinical Genetics, 2023
A de novo heterozygous POU3F3 genotype for the p.(Q214*) variant in a fetus with transient isolated bilateral mild ventriculomegaly: a case report and review of the literature.
Zhang H et al.
Frontiers in Pediatrics, 2023
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