PBX1突变致先天性肾和尿路异常综合征伴或不伴听力损失、耳朵异常或发育迟缓1例基因型及表型分析

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

摘要:

Abstract: