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Expert Review of Molecular Diagnostics|July 11, 2007
Emerging technologies for point-of-care genetic testingMark G Dobson, Paul Galvin, David E BartonScientific Reports|February 12, 2020
Investigation of DNA variants specific to ROBO2 Isoform 'a' in Irish vesicoureteric reflux patients reveals marked CpG island variationJohn M Darlow, Mark G Dobson, Andrew J Green, et al.Kidney International|March 29, 2013
Heterozygous non-synonymous ROBO2 variants are unlikely to be sufficient to cause familial vesicoureteric refluxMark G Dobson, John M Darlow, Manuela Hunziker, et al.Scientific Reports|January 10, 2018
Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric refluxJohn M Darlow, Rebecca Darlay, Mark G Dobson, et al.Scientific Reports|November 4, 2017
Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric refluxJohn M Darlow, Rebecca Darlay, Mark G Dobson, et al.Journal of the American Society of Nephrology : JASN|August 23, 2014
Urinary tract effects of HPSE2 mutationsHelen M Stuart, Neil A Roberts, Emma N Hilton, et al.Journal of the American Society of Nephrology : JASN|February 18, 2021
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral RefluxMiguel Verbitsky, Priya Krithivasan, Ekaterina Batourina, et al.Nature Genetics|December 23, 2018
The copy number variation landscape of congenital anomalies of the kidney and urinary tractMiguel Verbitsky, Rik Westland, Alejandra Perez, et al.Nature Genetics|March 1, 2019
Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tractMiguel Verbitsky, Rik Westland, Alejandra Perez, et al.Pageof 1