Associated Papers
Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohort.
Yang X et al.
Bmc Medical Genomics, 2021
34696790 (PubMed )
Supplement: 12920_2021_1102_MOESM1_ESM.pdf
PAX2 Mutation-Related Renal Hypodysplasia: Review of the Literature and Three Case Reports.
Chang YM et al.
Frontiers in Pediatrics, 2021
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