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Heiko Reutter

Showing results (131-140 of 209) with videos related to

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European Journal of Pediatrics|November 3, 2010
Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literatureCharlotte Schramm, Markus Draaken, Gabriel Tewes, et al.
American Journal of Medical Genetics. Part A|December 14, 2006
A family-based association study in Central Europeans: no evidence for the cystathionine beta-synthase c.844ins68 gene variant as a risk factor for non-syndromic cleft lip and palateStefanie Birnbaum, Heiko Reutter, Meinhard Mende, et al.
Children (Basel, Switzerland)|February 27, 2026
Burden of RSV-Associated Inpatient Care and Emergency Service Utilization in Two German Pediatric Centers Across Six Seasons Including the First Nirsevimab YearLisa Gürke, Gregor Hanslik, Linda-Marie Mulzer, et al.
Stroke|October 30, 2024
Ultrasound Localization Microscopy for the Assessment of Microvascular Circulation in Ischemic Perinatal StrokeAdrian P Regensburger, Felix Wachter, Louise Denis, et al.
Journal of Human Genetics|May 16, 2008
TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palateHeiko Reutter, Stefanie Birnbaum, Meinhard Mende, et al.
The Journal of Pediatrics|December 17, 2013
An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) associationBenjamin D Solomon, Linda A Baker, Kelly A Bear, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 25, 2014
Genome-wide mapping of copy number variations in patients with both anorectal malformations and central nervous system abnormalitiesGabriel C Dworschak, Markus Draaken, Alina C Hilger, et al.
Orphanet Journal of Rare Diseases|September 18, 2012
Assisted reproductive techniques and the risk of anorectal malformations: a German case-control studyNadine Zwink, Ekkehart Jenetzky, Eberhard Schmiedeke, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 6, 2013
Second study on the recurrence risk of isolated esophageal atresia with or without trachea-esophageal fistula among first-degree relatives: no evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association spectrumVera Choinitzki, Nadine Zwink, Enrika Bartels, et al.
International Journal of Molecular Medicine|March 25, 2011
Genome-wide expression profiling of urinary bladder implicates desmosomal and cytoskeletal dysregulation in the bladder exstrophy-epispadias complexLihong Qi, Kun Chen, David J Hur, et al.
Pageof 21

Showing results (131-140 of 209) with videos related to

Sort By:
Pageof 21
European Journal of Pediatrics|November 3, 2010
Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literatureCharlotte Schramm, Markus Draaken, Gabriel Tewes, et al.
American Journal of Medical Genetics. Part A|December 14, 2006
A family-based association study in Central Europeans: no evidence for the cystathionine beta-synthase c.844ins68 gene variant as a risk factor for non-syndromic cleft lip and palateStefanie Birnbaum, Heiko Reutter, Meinhard Mende, et al.
Children (Basel, Switzerland)|February 27, 2026
Burden of RSV-Associated Inpatient Care and Emergency Service Utilization in Two German Pediatric Centers Across Six Seasons Including the First Nirsevimab YearLisa Gürke, Gregor Hanslik, Linda-Marie Mulzer, et al.
Stroke|October 30, 2024
Ultrasound Localization Microscopy for the Assessment of Microvascular Circulation in Ischemic Perinatal StrokeAdrian P Regensburger, Felix Wachter, Louise Denis, et al.
Journal of Human Genetics|May 16, 2008
TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palateHeiko Reutter, Stefanie Birnbaum, Meinhard Mende, et al.
The Journal of Pediatrics|December 17, 2013
An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) associationBenjamin D Solomon, Linda A Baker, Kelly A Bear, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 25, 2014
Genome-wide mapping of copy number variations in patients with both anorectal malformations and central nervous system abnormalitiesGabriel C Dworschak, Markus Draaken, Alina C Hilger, et al.
Orphanet Journal of Rare Diseases|September 18, 2012
Assisted reproductive techniques and the risk of anorectal malformations: a German case-control studyNadine Zwink, Ekkehart Jenetzky, Eberhard Schmiedeke, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 6, 2013
Second study on the recurrence risk of isolated esophageal atresia with or without trachea-esophageal fistula among first-degree relatives: no evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association spectrumVera Choinitzki, Nadine Zwink, Enrika Bartels, et al.
International Journal of Molecular Medicine|March 25, 2011
Genome-wide expression profiling of urinary bladder implicates desmosomal and cytoskeletal dysregulation in the bladder exstrophy-epispadias complexLihong Qi, Kun Chen, David J Hur, et al.
Pageof 21