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Heiko Reutter

Showing results (171-180 of 209) with videos related to

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American Journal of Human Genetics|November 15, 2011
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like SyndromeStefanie Weber, Holger Thiele, Sevgi Mir, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 19, 2014
Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomaliesClaudia Zeidler, Joachim Woelfle, Markus Draaken, et al.
Birth Defects Research|March 3, 2018
Nonsyndromic cleft palate: An association study at GWAS candidate loci in a multiethnic sampleNina Ishorst, Paola Francheschelli, Anne C Böhmer, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|August 1, 2025
[Development of a standardized handover for critically ill premature and newborn infants for interhospital transport in Bavaria]Janik Wolff, Christian Batzlsperger, Christian Brickmann, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|December 9, 2025
[Correction: Development of a standardized handover for critically ill premature and newborn infants for interhospital transport in Bavaria]Janik Wolff, Christian Batzlsperger, Christian Brickmann, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 30, 2022
Definition, diagnosis and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet Working Group on Kidney MalformationsStefan Kohl, Fred E Avni, Peter Boor, et al.
American Journal of Human Genetics|May 22, 2012
Cantú syndrome is caused by mutations in ABCC9Bregje W M van Bon, Christian Gilissen, Dorothy K Grange, et al.
American Journal of Medical Genetics. Part A|September 17, 2013
De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL-like association and analysis of EFNB2 in patients with anorectal malformationsGabriel C Dworschak, Markus Draaken, Carlo Marcelis, 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.
The Journal of Pediatrics|June 18, 2011
Phenotype severity in the bladder exstrophy-epispadias complex: analysis of genetic and nongenetic contributing factors in 441 families from North America and EuropeHeiko Reutter, Simeon A Boyadjiev, Lisa Gambhir, et al.
Pageof 21

Showing results (171-180 of 209) with videos related to

Sort By:
Pageof 21
American Journal of Human Genetics|November 15, 2011
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like SyndromeStefanie Weber, Holger Thiele, Sevgi Mir, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 19, 2014
Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomaliesClaudia Zeidler, Joachim Woelfle, Markus Draaken, et al.
Birth Defects Research|March 3, 2018
Nonsyndromic cleft palate: An association study at GWAS candidate loci in a multiethnic sampleNina Ishorst, Paola Francheschelli, Anne C Böhmer, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|August 1, 2025
[Development of a standardized handover for critically ill premature and newborn infants for interhospital transport in Bavaria]Janik Wolff, Christian Batzlsperger, Christian Brickmann, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|December 9, 2025
[Correction: Development of a standardized handover for critically ill premature and newborn infants for interhospital transport in Bavaria]Janik Wolff, Christian Batzlsperger, Christian Brickmann, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 30, 2022
Definition, diagnosis and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet Working Group on Kidney MalformationsStefan Kohl, Fred E Avni, Peter Boor, et al.
American Journal of Human Genetics|May 22, 2012
Cantú syndrome is caused by mutations in ABCC9Bregje W M van Bon, Christian Gilissen, Dorothy K Grange, et al.
American Journal of Medical Genetics. Part A|September 17, 2013
De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL-like association and analysis of EFNB2 in patients with anorectal malformationsGabriel C Dworschak, Markus Draaken, Carlo Marcelis, 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.
The Journal of Pediatrics|June 18, 2011
Phenotype severity in the bladder exstrophy-epispadias complex: analysis of genetic and nongenetic contributing factors in 441 families from North America and EuropeHeiko Reutter, Simeon A Boyadjiev, Lisa Gambhir, et al.
Pageof 21