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Markus Stumm

Showing results (11-20 of 26) with videos related to

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Prenatal Diagnosis|March 3, 2007
Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosisMarkus Stumm, Eva Klopocki, Adam Gasiorek-Wiens, et al.
Carcinogenesis|July 16, 2002
Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemiaMartin Digweed, Susanne Rothe, Ilja Demuth, et al.
Radiation Research|February 13, 2002
Radiosensitivity of ataxia telangiectasia and Nijmegen breakage syndrome homozygotes and heterozygotes as determined by three-color FISH chromosome paintingSusann Neubauer, Rouben Arutyunyan, Markus Stumm, et al.
Cytogenetic and Genome Research|December 19, 2022
Intersexual Twins due to Tetragametic ChimerismRainer Wimmer, Uta Neumann, André Weber, et al.
Prenatal Diagnosis|September 2, 2014
Consanguinity and pregnancy outcomes in a multi-ethnic, metropolitan European populationRolf Becker, Thomas Keller, Rolf-Dieter Wegner, et al.
Prenatal Diagnosis|May 11, 2012
Noninvasive prenatal detection of chromosomal aneuploidies using different next generation sequencing strategies and algorithmsMarkus Stumm, Michael Entezami, Nastasja Trunk, et al.
Cell Cycle (Georgetown, Tex.)|December 15, 2010
MCPH1 patient cells exhibit delayed release from DNA damage-induced G2/M checkpoint arrestIoannis Gavvovidis, Charlotte Pöhlmann, Juan Alberto Marchal, et al.
Journal of Clinical Medicine|August 4, 2015
Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing TwinsSebastian Grömminger, Erbil Yagmur, Sanli Erkan, et al.
American Journal of Human Genetics|May 5, 2009
Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorderRegina Waltes, Reinhard Kalb, Magtouf Gatei, et al.
American Journal of Human Genetics|February 9, 2010
Warsaw breakage syndrome, a cohesinopathy associated with mutations in the XPD helicase family member DDX11/ChlR1Petra van der Lelij, Krystyna H Chrzanowska, Barbara C Godthelp, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Prenatal Diagnosis|March 3, 2007
Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosisMarkus Stumm, Eva Klopocki, Adam Gasiorek-Wiens, et al.
Carcinogenesis|July 16, 2002
Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemiaMartin Digweed, Susanne Rothe, Ilja Demuth, et al.
Radiation Research|February 13, 2002
Radiosensitivity of ataxia telangiectasia and Nijmegen breakage syndrome homozygotes and heterozygotes as determined by three-color FISH chromosome paintingSusann Neubauer, Rouben Arutyunyan, Markus Stumm, et al.
Cytogenetic and Genome Research|December 19, 2022
Intersexual Twins due to Tetragametic ChimerismRainer Wimmer, Uta Neumann, André Weber, et al.
Prenatal Diagnosis|September 2, 2014
Consanguinity and pregnancy outcomes in a multi-ethnic, metropolitan European populationRolf Becker, Thomas Keller, Rolf-Dieter Wegner, et al.
Prenatal Diagnosis|May 11, 2012
Noninvasive prenatal detection of chromosomal aneuploidies using different next generation sequencing strategies and algorithmsMarkus Stumm, Michael Entezami, Nastasja Trunk, et al.
Cell Cycle (Georgetown, Tex.)|December 15, 2010
MCPH1 patient cells exhibit delayed release from DNA damage-induced G2/M checkpoint arrestIoannis Gavvovidis, Charlotte Pöhlmann, Juan Alberto Marchal, et al.
Journal of Clinical Medicine|August 4, 2015
Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing TwinsSebastian Grömminger, Erbil Yagmur, Sanli Erkan, et al.
American Journal of Human Genetics|May 5, 2009
Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorderRegina Waltes, Reinhard Kalb, Magtouf Gatei, et al.
American Journal of Human Genetics|February 9, 2010
Warsaw breakage syndrome, a cohesinopathy associated with mutations in the XPD helicase family member DDX11/ChlR1Petra van der Lelij, Krystyna H Chrzanowska, Barbara C Godthelp, et al.
Pageof 3