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Bernhard G Herrmann

Showing results (51-60 of 60) with videos related to

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Birth Defects Research. Part A, Clinical and Molecular Teratology|January 30, 2013
Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12Markus Draaken, Sadaf S Mughal, Tracie Pennimpede, et al.
Plos One|January 5, 2011
Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysisBernd Timmermann, Martin Kerick, Christina Roehr, et al.
Plos Genetics|March 13, 2015
Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophyMarkus Draaken, Michael Knapp, Tracie Pennimpede, et al.
European Journal of Human Genetics : EJHG|April 4, 2013
De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL associationAlina Hilger, Charlotte Schramm, Tracie Pennimpede, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 26, 2014
Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical regionMarkus Draaken, Friederike Baudisch, Bernd Timmermann, et al.
Human Genetics|June 1, 2015
Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tractDaw-Yang Hwang, Stefan Kohl, Xueping Fan, et al.
Human Molecular Genetics|May 24, 2014
Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladderHeiko Reutter, Markus Draaken, Tracie Pennimpede, et al.
Kidney International|October 25, 2013
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL associationPawaree Saisawat, Stefan Kohl, Alina C Hilger, et al.
Nature Biotechnology|March 11, 2008
Minimum information specification for in situ hybridization and immunohistochemistry experiments (MISFISHIE)Eric W Deutsch, Catherine A Ball, Jules J Berman, et al.
HGG Advances|February 24, 2022
First genome-wide association study of esophageal atresia identifies three genetic risk loci at <i>CTNNA3</i>, <i>FOXF1</i>/<i>FOXC2</i>/<i>FOXL1</i>, and <i>HNF1B</i>Jan Gehlen, Ann-Sophie Giel, Ricarda Köllges, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 30, 2013
Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12Markus Draaken, Sadaf S Mughal, Tracie Pennimpede, et al.
Plos One|January 5, 2011
Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysisBernd Timmermann, Martin Kerick, Christina Roehr, et al.
Plos Genetics|March 13, 2015
Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophyMarkus Draaken, Michael Knapp, Tracie Pennimpede, et al.
European Journal of Human Genetics : EJHG|April 4, 2013
De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL associationAlina Hilger, Charlotte Schramm, Tracie Pennimpede, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 26, 2014
Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical regionMarkus Draaken, Friederike Baudisch, Bernd Timmermann, et al.
Human Genetics|June 1, 2015
Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tractDaw-Yang Hwang, Stefan Kohl, Xueping Fan, et al.
Human Molecular Genetics|May 24, 2014
Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladderHeiko Reutter, Markus Draaken, Tracie Pennimpede, et al.
Kidney International|October 25, 2013
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL associationPawaree Saisawat, Stefan Kohl, Alina C Hilger, et al.
Nature Biotechnology|March 11, 2008
Minimum information specification for in situ hybridization and immunohistochemistry experiments (MISFISHIE)Eric W Deutsch, Catherine A Ball, Jules J Berman, et al.
HGG Advances|February 24, 2022
First genome-wide association study of esophageal atresia identifies three genetic risk loci at <i>CTNNA3</i>, <i>FOXF1</i>/<i>FOXC2</i>/<i>FOXL1</i>, and <i>HNF1B</i>Jan Gehlen, Ann-Sophie Giel, Ricarda Köllges, et al.
Pageof 6