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Martin Zenker

Showing results (211-220 of 338) with videos related to

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European Journal of Human Genetics : EJHG|July 9, 2015
Loss-of-function variants in HIVEP2 are a cause of intellectual disabilitySiddharth Srivastava, Hartmut Engels, Ina Schanze, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 11, 2007
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)Rasheed Gbadegesin, Bernward G Hinkes, Bethan E Hoskins, et al.
American Journal of Medical Genetics. Part A|October 12, 2013
Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS-FREM complex disordersDenny Schanze, Magdalena Harakalova, Cathy A Stevens, et al.
Clinical Dysmorphology|June 11, 2008
No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndromeBenjamin Abo-Dalo, Melanie Roes, Sonia Canún, et al.
Pediatric Nephrology (Berlin, Germany)|July 3, 2008
Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndromeAndreas Dietrich, Verena Matejas, Martin Bitzan, et al.
Journal of Medical Genetics|April 19, 2012
Mutations in GRIP1 cause Fraser syndromeMaartje J Vogel, Patrick van Zon, Louise Brueton, et al.
Signal Transduction and Targeted Therapy|January 4, 2026
Immunoglobulin heavy-chain status and stromal interactions shape ferroptosis sensitivity in chronic lymphocytic leukemiaMartin Böttcher, Lea Reemts, Paul J Hengeveld, et al.
Journal of Medical Genetics|July 3, 2007
Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arraysJuliane Hoyer, Alexander Dreweke, Christian Becker, et al.
European Journal of Medical Genetics|November 4, 2022
Intrafamilial phenotypic variability in autosomal recessive DOCK6-related Adams-Oliver syndromeLuz Consuelo Zepeda-Romero, Martin Zenker, Denny Schanze, et al.
Pediatric Neurology|March 31, 2026
Truncating Variants in KIF5C Cause a Milder Disorder Distinct From KIF5C-Associated Cortical DysplasiaLuise Kulosik, Ina Schanze, Pia Zacher, et al.
Pageof 34

Showing results (211-220 of 338) with videos related to

Sort By:
Pageof 34
European Journal of Human Genetics : EJHG|July 9, 2015
Loss-of-function variants in HIVEP2 are a cause of intellectual disabilitySiddharth Srivastava, Hartmut Engels, Ina Schanze, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 11, 2007
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)Rasheed Gbadegesin, Bernward G Hinkes, Bethan E Hoskins, et al.
American Journal of Medical Genetics. Part A|October 12, 2013
Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS-FREM complex disordersDenny Schanze, Magdalena Harakalova, Cathy A Stevens, et al.
Clinical Dysmorphology|June 11, 2008
No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndromeBenjamin Abo-Dalo, Melanie Roes, Sonia Canún, et al.
Pediatric Nephrology (Berlin, Germany)|July 3, 2008
Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndromeAndreas Dietrich, Verena Matejas, Martin Bitzan, et al.
Journal of Medical Genetics|April 19, 2012
Mutations in GRIP1 cause Fraser syndromeMaartje J Vogel, Patrick van Zon, Louise Brueton, et al.
Signal Transduction and Targeted Therapy|January 4, 2026
Immunoglobulin heavy-chain status and stromal interactions shape ferroptosis sensitivity in chronic lymphocytic leukemiaMartin Böttcher, Lea Reemts, Paul J Hengeveld, et al.
Journal of Medical Genetics|July 3, 2007
Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arraysJuliane Hoyer, Alexander Dreweke, Christian Becker, et al.
European Journal of Medical Genetics|November 4, 2022
Intrafamilial phenotypic variability in autosomal recessive DOCK6-related Adams-Oliver syndromeLuz Consuelo Zepeda-Romero, Martin Zenker, Denny Schanze, et al.
Pediatric Neurology|March 31, 2026
Truncating Variants in KIF5C Cause a Milder Disorder Distinct From KIF5C-Associated Cortical DysplasiaLuise Kulosik, Ina Schanze, Pia Zacher, et al.
Pageof 34