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Filters: Author is Wu, Chen-Han Wilfred and Keyword is Eye Abnormalities  [Clear All Filters]
2020
Wu, C. - H. Wilfred et al. Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT). Genet Med 22, 1673-1681 (2020).