Associated Papers
Multilocus Disease-Causing Genomic Variations for Genetic Disorders: Single Tertiary Centre Experience From Türkiye.
Kablan A et al.
Clinical Genetics, 2025
Novel de novo pathogenic variant in the NR2F2 gene in a boy with congenital heart defect and dysmorphic features.
Upadia J et al.
American Journal of Medical Genetics. Part A, 2018
Rare variants in NR2F2 cause congenital heart defects in humans.
Al Turki S et al.
American Journal of Human Genetics, 2014
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