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Michael Ludwig

Showing results (231-240 of 239) with videos related to

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Plos One|May 29, 2019
Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformationsRomy van de Putte, Charlotte H W Wijers, Heiko Reutter, et al.
Scientific Reports|February 9, 2017
ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract developmentRong Zhang, Michael Knapp, Kentaro Suzuki, et al.
American Journal of Human Genetics|May 4, 2019
Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract ObstructionCaroline M Kolvenbach, Gabriel C Dworschak, Sandra Frese, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 7, 2016
Long-term renal outcome in children with OCRL mutations: retrospective analysis of a large international cohortMarcin Zaniew, Arend Bökenkamp, Marcin Kolbuc, et al.
Plos One|June 6, 2020
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresiaRong Zhang, Jan Gehlen, Amit Kawalia, et al.
Frontiers in Cell and Developmental Biology|August 28, 2020
<i>SLC20A1</i> Is Involved in Urinary Tract and Urorectal DevelopmentJohanna Magdalena Rieke, Rong Zhang, Doreen Braun, et al.
Cell|January 6, 2015
Organoid models of human and mouse ductal pancreatic cancerSylvia F Boj, Chang-Il Hwang, Lindsey A Baker, et al.
Communications Biology|November 9, 2022
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophyEnrico Mingardo, Glenda Beaman, Philip Grote, 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 24

Showing results (231-240 of 239) with videos related to

Sort By:
Pageof 24
You have reached the last page of results.This site can display upto 239 results.
Plos One|May 29, 2019
Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformationsRomy van de Putte, Charlotte H W Wijers, Heiko Reutter, et al.
Scientific Reports|February 9, 2017
ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract developmentRong Zhang, Michael Knapp, Kentaro Suzuki, et al.
American Journal of Human Genetics|May 4, 2019
Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract ObstructionCaroline M Kolvenbach, Gabriel C Dworschak, Sandra Frese, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 7, 2016
Long-term renal outcome in children with OCRL mutations: retrospective analysis of a large international cohortMarcin Zaniew, Arend Bökenkamp, Marcin Kolbuc, et al.
Plos One|June 6, 2020
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresiaRong Zhang, Jan Gehlen, Amit Kawalia, et al.
Frontiers in Cell and Developmental Biology|August 28, 2020
<i>SLC20A1</i> Is Involved in Urinary Tract and Urorectal DevelopmentJohanna Magdalena Rieke, Rong Zhang, Doreen Braun, et al.
Cell|January 6, 2015
Organoid models of human and mouse ductal pancreatic cancerSylvia F Boj, Chang-Il Hwang, Lindsey A Baker, et al.
Communications Biology|November 9, 2022
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophyEnrico Mingardo, Glenda Beaman, Philip Grote, 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 24