Wu Liting, Shi Yu, Huang Daochao, Wu Rui, Li Shuxiang, Zhou Quansheng, Gui Junfeng, Cai Yiqing, Song Cui. Genotype and phenotype analysis of a case of congenital anomalies of kidney and urinary tract syndrome with or without hearing loss，abnormal ears or developmental delay caused by PBX1 mutation[J]. Journal of Chongqing Medical University,2022,47(3):358-362
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