Associated Papers
FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia.
Pendleton KE et al.
Journal of Pediatric Genetics, 2024
FOXP3 mutations causing early-onset insulin-requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Hwang JL et al.
Pediatric Diabetes, 2018
Phenotypic heterogeneity in monogenic diabetes: the clinical and diagnostic utility of a gene panel-based next-generation sequencing approach.
Alkorta-Aranburu G et al.
Molecular Genetics and Metabolism, 2014
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