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2. Copy-Number Disorders Are a Common Cause of Congenital Kidney Malformations

3. Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome

4. Localization of a Gene for Nonsyndromic Renal Hypodysplasia to Chromosome 1p32-33

5. Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis

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