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Heiko Reutter

Showing results (151-160 of 209) with videos related to

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American Journal of Medical Genetics. Part A|February 28, 2012
A phenotype map for 14q32.3 terminal deletionsHartmut Engels, Herdit M Schüler, Alexander M Zink, et al.
American Journal of Human Genetics|April 30, 2013
Yunis-Varón syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatasePhilippe M Campeau, Guy M Lenk, James T Lu, et al.
Pediatric Surgery International|May 15, 2012
Inheritance of the VATER/VACTERL associationEnrika Bartels, Ekkehart Jenetzky, Benjamin D Solomon, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
De novo duplication of 18p11.21-18q12.1 in a female with anorectal malformationCharlotte Schramm, Markus Draaken, Enrika Bartels, et al.
Human Mutation|August 22, 2015
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL AssociationAlina C Hilger, Jan Halbritter, Tracie Pennimpede, et al.
Genes|September 28, 2021
Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO)Luca M Schierbaum, Sophia Schneider, Stefan Herms, et al.
Birth Defects Research|April 1, 2022
Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformationCorina E Thiem, Jil D Stegmann, Alina C Hilger, et al.
BMC Medical Genetics|May 4, 2016
CNV analysis in 169 patients with bladder exstrophy-epispadias complexCatharina von Lowtzow, Andrea Hofmann, Rong Zhang, et al.
Wiener Medizinische Wochenschrift (1946)|August 8, 2022
Umbilical venous catheter- and peripherally inserted central catheter-associated complications in preterm infants with birth weight < 1250 g : Results from a survey in Austria and GermanySteffi Hess, Martin Poryo, Ralf Böttger, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|February 3, 2025
Ultrasound Super-Resolution Imaging of Neonatal Cerebral Vascular ReorganizationSimone Schwarz, Louise Denis, Emmanuel Nedoschill, et al.
Pageof 21

Showing results (151-160 of 209) with videos related to

Sort By:
Pageof 21
American Journal of Medical Genetics. Part A|February 28, 2012
A phenotype map for 14q32.3 terminal deletionsHartmut Engels, Herdit M Schüler, Alexander M Zink, et al.
American Journal of Human Genetics|April 30, 2013
Yunis-Varón syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatasePhilippe M Campeau, Guy M Lenk, James T Lu, et al.
Pediatric Surgery International|May 15, 2012
Inheritance of the VATER/VACTERL associationEnrika Bartels, Ekkehart Jenetzky, Benjamin D Solomon, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
De novo duplication of 18p11.21-18q12.1 in a female with anorectal malformationCharlotte Schramm, Markus Draaken, Enrika Bartels, et al.
Human Mutation|August 22, 2015
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL AssociationAlina C Hilger, Jan Halbritter, Tracie Pennimpede, et al.
Genes|September 28, 2021
Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO)Luca M Schierbaum, Sophia Schneider, Stefan Herms, et al.
Birth Defects Research|April 1, 2022
Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformationCorina E Thiem, Jil D Stegmann, Alina C Hilger, et al.
BMC Medical Genetics|May 4, 2016
CNV analysis in 169 patients with bladder exstrophy-epispadias complexCatharina von Lowtzow, Andrea Hofmann, Rong Zhang, et al.
Wiener Medizinische Wochenschrift (1946)|August 8, 2022
Umbilical venous catheter- and peripherally inserted central catheter-associated complications in preterm infants with birth weight < 1250 g : Results from a survey in Austria and GermanySteffi Hess, Martin Poryo, Ralf Böttger, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|February 3, 2025
Ultrasound Super-Resolution Imaging of Neonatal Cerebral Vascular ReorganizationSimone Schwarz, Louise Denis, Emmanuel Nedoschill, et al.
Pageof 21