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All mouse models of congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay with phenotypic similarity to the human disease
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay | Pbx1em1Dunw/Pbx1em1Dunw | C57BL/6J-Pbx1em1Dunw | J:320934 | View |