Pages that link to "Q42653487"
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The following pages link to Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds (Q42653487):
Displaying 39 items.
- Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux (Q24300041) (← links)
- Vesico-ureteric reflux and urinary tract development in the Pax2 1Neu /- mouse (Q28584800) (← links)
- The use of grid computing to drive data-intensive genetic research (Q31106493) (← links)
- Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux (Q33562267) (← links)
- Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients. (Q34256093) (← links)
- A genome scan in affected sib-pairs with familial vesicoureteral reflux identifies a locus on chromosome 5 (Q34328556) (← links)
- Urinary tract infection in children: recurrent infections (Q35661437) (← links)
- Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33 (Q35677743) (← links)
- Linkage study of 14 candidate genes and loci in four large Dutch families with vesico-ureteral reflux (Q35884248) (← links)
- Genetic approaches to human renal agenesis/hypoplasia and dysplasia (Q36013624) (← links)
- New congenital anomalies of the kidney and urinary tract and outcomes in Robo2 mutant mice with the inserted piggyBac transposon (Q36086539) (← links)
- A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity (Q36484807) (← links)
- Genetics of Vesicoureteral Reflux (Q36658504) (← links)
- ROBO2 gene variants are associated with familial vesicoureteral reflux (Q36666892) (← links)
- Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney. (Q36807618) (← links)
- Genetic contribution and associated pathophysiology in end-stage renal disease (Q36925161) (← links)
- Analysis of the IL-10, IL-12, and TNF-α Gene Polymorphisms in Patients With Vesicoureteral Reflux Among the Southeast Iranian Population (Q36945338) (← links)
- Gene discovery and vesicoureteric reflux (Q37078188) (← links)
- Renal tract malformations: perspectives for nephrologists (Q37150737) (← links)
- Clinical and genetic features of a dominantly-inherited microphthalmia pedigree from China. (Q37194566) (← links)
- A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13. (Q37259295) (← links)
- A genome-wide scan for genes involved in primary vesicoureteric reflux. (Q37363254) (← links)
- The genetics of primary, nonsyndromic vesicoureteral reflux (Q37862963) (← links)
- Vesicoureteric reflux and reflux nephropathy: from mouse models to childhood disease (Q38185597) (← links)
- Genetics of vesicoureteral reflux. (Q39485603) (← links)
- Five cases of severe vesico-ureteric reflux in a family with an X-linked compatible trait (Q39952614) (← links)
- Annotated chromosome maps for renal disease (Q40018059) (← links)
- Genome gender diversity in affected sib‐pairs with familial vesico‐ureteric reflux identified by single nucleotide polymorphism linkage analysis (Q44770698) (← links)
- Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux (Q45138496) (← links)
- RET Gly691Ser mutation is associated with primary vesicoureteral reflux in the French-Canadian population from Quebec. (Q46754712) (← links)
- Genetic basis of human congenital anomalies of the kidney and urinary tract (Q47224735) (← links)
- Mutations in the ROBO2 and SLIT2 genes are rare causes of familial vesico-ureteral reflux (Q51731897) (← links)
- Embryology and genetics of primary vesico-ureteric reflux and associated renal dysplasia. (Q51997234) (← links)
- ROBO2 gene variants in children with primary nonsyndromic vesicoureteral reflux with or without renal hypoplasia/dysplasia. (Q53979458) (← links)
- Congenital Disorders of the Human Urinary Tract: Recent Insights From Genetic and Molecular Studies (Q64054916) (← links)
- Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14 (Q81412189) (← links)
- Vesico-ureteric reflux: using mouse models to understand a common congenital urinary tract defect (Q83674232) (← links)
- The C3H/HeJ inbred mouse is a model of vesico-ureteric reflux with a susceptibility locus on chromosome 12 (Q84083024) (← links)
- DNA copy number variations in children with vesicoureteral reflux and urinary tract infections (Q92564236) (← links)