학술논문
Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)
Document Type
Article
Author
Wu, Chen-Han Wilfred; Mann, Nina; Nakayama, Makiko; Connaughton, Dervla M.; Dai, Rufeng; Kolvenbach, Caroline M.; Kause, Franziska; Ottlewski, Isabel; Wang, Chunyan; Klämbt, Verena; Seltzsam, Steve; Lai, Ethan W.; Selvin, Aravind; Senguttuva, Prabha; Bodamer, Olaf; Stein, Deborah R.; El Desoky, Sherif; Kari, Jameela A.; Tasic, Velibor; Bauer, Stuart B.; Shril, Shirlee; Hildebrandt, Friedhelm
Source
In Genetics in Medicine October 2020 22(10):1673-1681
Subject
Language
ISSN
1098-3600