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Heiko Reutter

Showing results (141-150 of 209) with videos related to

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European Journal of Human Genetics : EJHG|April 27, 2022
Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidate genesKatinka Breuer, Korbinian M Riedhammer, Nicole Müller, et al.
Journal of Pediatric Surgery|December 10, 2013
First results of a European multi-center registry of patients with anorectal malformationsIvo de Blaauw, Charlotte H W Wijers, Eberhard Schmiedeke, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|January 7, 2017
Esophageal Atresia with or without Tracheoesophageal Fistula (EA/TEF): Association of Different EA/TEF Subtypes with Specific Co-occurring Congenital Anomalies and Implications for Diagnostic WorkupThomas Bogs, Nadine Zwink, Vera Chonitzki, et al.
European Journal of Oral Sciences|March 27, 2009
Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palateStefanie Birnbaum, Heiko Reutter, Meinhard Mende, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 31, 2012
Nine new twin pairs with esophageal atresia: a review of the literature and performance of a twin study of the disorderAnna Carina Schulz, Enrika Bartels, Rüdiger Stressig, et al.
Birth Defects Research|February 2, 2018
Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate geneValerie Weitensteiner, Rong Zhang, Julia Bungenberg, et al.
International Journal of Pediatric Otorhinolaryngology|July 10, 2009
Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descentHeiko Reutter, Stefanie Birnbaum, Meinhard Mende, et al.
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.
International Journal of Pediatric Otorhinolaryngology|November 4, 2010
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patientsNilma Almeida de Assis, Stefanie Nowak, Kerstin U Ludwig, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|October 23, 2025
Sensing ultrasound localization microscopy for ultrastructural and functional imaging of neonatal kidneysHenriette Grieshaber-Bouyer Mandelbaum, Felix Wachter, Louise Denis, et al.
Pageof 21

Showing results (141-150 of 209) with videos related to

Sort By:
Pageof 21
European Journal of Human Genetics : EJHG|April 27, 2022
Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidate genesKatinka Breuer, Korbinian M Riedhammer, Nicole Müller, et al.
Journal of Pediatric Surgery|December 10, 2013
First results of a European multi-center registry of patients with anorectal malformationsIvo de Blaauw, Charlotte H W Wijers, Eberhard Schmiedeke, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|January 7, 2017
Esophageal Atresia with or without Tracheoesophageal Fistula (EA/TEF): Association of Different EA/TEF Subtypes with Specific Co-occurring Congenital Anomalies and Implications for Diagnostic WorkupThomas Bogs, Nadine Zwink, Vera Chonitzki, et al.
European Journal of Oral Sciences|March 27, 2009
Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palateStefanie Birnbaum, Heiko Reutter, Meinhard Mende, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 31, 2012
Nine new twin pairs with esophageal atresia: a review of the literature and performance of a twin study of the disorderAnna Carina Schulz, Enrika Bartels, Rüdiger Stressig, et al.
Birth Defects Research|February 2, 2018
Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate geneValerie Weitensteiner, Rong Zhang, Julia Bungenberg, et al.
International Journal of Pediatric Otorhinolaryngology|July 10, 2009
Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descentHeiko Reutter, Stefanie Birnbaum, Meinhard Mende, et al.
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.
International Journal of Pediatric Otorhinolaryngology|November 4, 2010
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patientsNilma Almeida de Assis, Stefanie Nowak, Kerstin U Ludwig, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|October 23, 2025
Sensing ultrasound localization microscopy for ultrastructural and functional imaging of neonatal kidneysHenriette Grieshaber-Bouyer Mandelbaum, Felix Wachter, Louise Denis, et al.
Pageof 21