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A Leutner

Showing results (1-10 of 9) with videos related to

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European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|November 16, 2004
Prolonged stenting does not prevent obstruction after TIP repair when the glans was deeply incisedC Lorenz, A Schmedding, A Leutner, et al.
Human Molecular Genetics|October 1, 1993
Dinucleotide repeat polymorphism at the D12S371 locusA Leutner, J Schönling, N K Spurr, et al.
Human Molecular Genetics|October 1, 1993
Dinucleotide repeat polymorphism at the D5S214 locusE Pick, A Leutner, N K Spurr, et al.
Studies in Health Technology and Informatics|September 21, 2021
Development of a Dashboard for Rare Diseases - A Technical Case ReportLiz A Leutner, Franziska Bathelt, Brita Sedlmayr, et al.
Studies in Health Technology and Informatics|May 27, 2021
Adaption of the OMOP CDM for Rare DiseasesMichele Zoch, Christian Gierschner, Yuan Peng, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Efficiency of various strategies and materials to generate new markers: saturating the region 5q11.2-q13.3 with 30 new randomly distributed clonesB Wirth, J Schönling, A el-Agwany, et al.
Health Informatics Journal|June 10, 2024
Transition database for rare diseases and its use for clinical documentationMichele Zoch, Christian Gierschner, Richard Gebler, et al.
Genomics|March 1, 1994
Large linkage analysis in 100 families with autosomal recessive spinal muscular atrophy (SMA) and 11 CEPH families using 15 polymorphic loci in the region 5q11.2-q13.3B Wirth, E Pick, A Leutner, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|November 7, 2015
Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German familiesN Zwink, V Choinitzki, F Baudisch, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|November 16, 2004
Prolonged stenting does not prevent obstruction after TIP repair when the glans was deeply incisedC Lorenz, A Schmedding, A Leutner, et al.
Human Molecular Genetics|October 1, 1993
Dinucleotide repeat polymorphism at the D12S371 locusA Leutner, J Schönling, N K Spurr, et al.
Human Molecular Genetics|October 1, 1993
Dinucleotide repeat polymorphism at the D5S214 locusE Pick, A Leutner, N K Spurr, et al.
Studies in Health Technology and Informatics|September 21, 2021
Development of a Dashboard for Rare Diseases - A Technical Case ReportLiz A Leutner, Franziska Bathelt, Brita Sedlmayr, et al.
Studies in Health Technology and Informatics|May 27, 2021
Adaption of the OMOP CDM for Rare DiseasesMichele Zoch, Christian Gierschner, Yuan Peng, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Efficiency of various strategies and materials to generate new markers: saturating the region 5q11.2-q13.3 with 30 new randomly distributed clonesB Wirth, J Schönling, A el-Agwany, et al.
Health Informatics Journal|June 10, 2024
Transition database for rare diseases and its use for clinical documentationMichele Zoch, Christian Gierschner, Richard Gebler, et al.
Genomics|March 1, 1994
Large linkage analysis in 100 families with autosomal recessive spinal muscular atrophy (SMA) and 11 CEPH families using 15 polymorphic loci in the region 5q11.2-q13.3B Wirth, E Pick, A Leutner, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|November 7, 2015
Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German familiesN Zwink, V Choinitzki, F Baudisch, et al.
Pageof 1