A single-center cohort of Canadian children with VUR reveals renal phenotypes important for genetic studies.

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Developmental Genetics and Congenital Anomalies of the Kidney and Urinary Tract.Heterozygous loss-of-function mutation in Odd-skipped related 1 (Osr1) is associated with vesicoureteric reflux, duplex systems, and hydronephrosis.

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A single-center cohort of Canadian children with VUR reveals renal phenotypes important for genetic studies.

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A single-center cohort of Cana ...... important for genetic studies.

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A single-center cohort of Cana ...... important for genetic studies.

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A single-center cohort of Cana ...... important for genetic studies.

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P1476

A single-center cohort of Cana ...... important for genetic studies

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Indra R Gupta

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Inga J Murawski

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Jasmine El Andalousi

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John-Paul Capolicchio

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Mohamed El-Sherbiny

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P2860

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes

Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux

Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux

Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1.

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

A genome scan in affected sib-pairs with familial vesicoureteral reflux identifies a locus on chromosome 5

Vesicoureteral reflux and reflux nephropathy.

Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33

Linkage study of 14 candidate genes and loci in four large Dutch families with vesico-ureteral reflux.

A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity.

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s00467-013-2440-9

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1813-1819

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scholarly article

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10.1007/S00467-013-2440-9

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Roman Jednak

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2013-03-26T00:00:00Z

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1006369795

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23529638

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A single-center cohort of Canadian children with VUR reveals renal phenotypes important for genetic studies.

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P2860

P2860

A single-center cohort of Canadian children with VUR reveals renal phenotypes important for genetic studies.

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