Showing results (21-30 of 31) with videos related to
Sort By:
Pageof 4
Plos One|June 25, 2011
In search of an uncultured human-associated TM7 bacterium in the environmentJorge M Dinis, David E Barton, Jamsheed Ghadiri, et al.European Journal of Human Genetics : EJHG|August 15, 2013
Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic)Mireille Claustres, Viktor Kožich, Els Dequeker, et al.European Journal of Human Genetics : EJHG|August 26, 2010
Preparation and validation of the first WHO international genetic reference panel for Fragile X syndromeMalcolm Hawkins, Jennifer Boyle, Kathleen E Wright, 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.Familial Cancer|July 10, 2012
Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndromeMichael P Farrell, David J Hughes, Ian R Berry, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 26, 2005
Developing a sustainable process to provide quality control materials for genetic testingBin Chen, Catherine D O' Connell, D Joe Boone, 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.Pageof 4