Genetic locus on chromosome 6p for multicystic renal dysplasia, pelvi-ureteral junction stenosis, and vesicoureteral reflux
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference11 articles.
1. Subclavian artery supply disruption sequence: Hypothesis of a vascular etiology for Poland, Klippel-Feil, and Möbius anomalies
2. Vesicoureteric reflux: Segregation analysis
3. The Multicystic Dysplastic Kidney and Contralateral Vesicoureteral Reflux: Protection of the Solitary Kidney
4. Hereditary hydronephrosis and the short arm of chromosome 6
5. Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6p
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1. A 12Mb deletion of 6p24.1→pter in an 18-gestational-week fetus with orofacial clefting, the Dandy–Walker malformation and bilateral multicystic kidneys;European Journal of Medical Genetics;2009-01
2. Primary ureteral reflux: emerging insights from molecular and genetic studies;Current Opinion in Pediatrics;2003-04
3. Poor predictability of prenatal ultrasonography for a nonfunctional kidney;Urology;2002-10
4. Multicystic dysplastic kidney and Kallmann's syndrome: a new association?;Nephrology Dialysis Transplantation;2001-06-01
5. Renal dysplasia in boxers and Finnish harriers;Journal of Small Animal Practice;2000-09
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