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Peter Nürnberg

Showing results (21-30 of 517) with videos related to

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European Journal of Human Genetics : EJHG|February 5, 2009
A novel VPS13B mutation in two brothers with Cohen syndrome, cutis verticis gyrata and sensorineural deafnessAndré Mégarbané, Rima Slim, Gudrun Nürnberg, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|June 15, 2007
Analysis of mitochondrial DNA in discordant monozygotic twins with neurofibromatosis type 1Anne Katrin Detjen, Sigrid Tinschert, Dieter Kaufmann, et al.
Electrophoresis|February 4, 2005
Genome-wide single-nucleotide polymorphism arrays demonstrate high fidelity of multiple displacement-based whole-genome amplificationMladen V Tzvetkov, Christian Becker, Bettina Kulle, et al.
Virology|December 7, 2007
Co-replication analyses of naturally occurring defective hepatitis B virus variants with wild-typeStefanie Märschenz, Anja Brinckmann, Peter Nürnberg, et al.
Epilepsia|January 21, 2016
Nocturnal frontal lobe epilepsy caused by a mutation in the GATOR1 complex gene NPRL3Georg-Christoph Korenke, Marlene Eggert, Holger Thiele, et al.
Investigative Ophthalmology & Visual Science|February 3, 2009
Comprehensive mutational screening in a cohort of Danish families with hereditary congenital cataractLars Hansen, Annemette Mikkelsen, Peter Nürnberg, et al.
Molecular Vision|November 18, 2006
A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian originVanita Vanita, Hans Christian Hennies, Daljit Singh, et al.
Electrophoresis|November 28, 2007
Detection of novel NF1 mutations and rapid mutation prescreening with PyrosequencingAnja Brinckmann, Claudia Mischung, Ingelore Bässmann, et al.
Proceedings. Biological Sciences|July 17, 2004
A longitudinal analysis of reproductive skew in male rhesus macaquesAnja Widdig, Fred B Bercovitch, Wolf Jürgen Streich, et al.
Biological Chemistry|March 30, 2016
A systematic comparison of two new releases of exome sequencing products: the aim of use determines the choice of productJanine Altmüller, Susanne Motameny, Christian Becker, et al.
Pageof 52

Showing results (21-30 of 517) with videos related to

Sort By:
Pageof 52
European Journal of Human Genetics : EJHG|February 5, 2009
A novel VPS13B mutation in two brothers with Cohen syndrome, cutis verticis gyrata and sensorineural deafnessAndré Mégarbané, Rima Slim, Gudrun Nürnberg, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|June 15, 2007
Analysis of mitochondrial DNA in discordant monozygotic twins with neurofibromatosis type 1Anne Katrin Detjen, Sigrid Tinschert, Dieter Kaufmann, et al.
Electrophoresis|February 4, 2005
Genome-wide single-nucleotide polymorphism arrays demonstrate high fidelity of multiple displacement-based whole-genome amplificationMladen V Tzvetkov, Christian Becker, Bettina Kulle, et al.
Virology|December 7, 2007
Co-replication analyses of naturally occurring defective hepatitis B virus variants with wild-typeStefanie Märschenz, Anja Brinckmann, Peter Nürnberg, et al.
Epilepsia|January 21, 2016
Nocturnal frontal lobe epilepsy caused by a mutation in the GATOR1 complex gene NPRL3Georg-Christoph Korenke, Marlene Eggert, Holger Thiele, et al.
Investigative Ophthalmology & Visual Science|February 3, 2009
Comprehensive mutational screening in a cohort of Danish families with hereditary congenital cataractLars Hansen, Annemette Mikkelsen, Peter Nürnberg, et al.
Molecular Vision|November 18, 2006
A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian originVanita Vanita, Hans Christian Hennies, Daljit Singh, et al.
Electrophoresis|November 28, 2007
Detection of novel NF1 mutations and rapid mutation prescreening with PyrosequencingAnja Brinckmann, Claudia Mischung, Ingelore Bässmann, et al.
Proceedings. Biological Sciences|July 17, 2004
A longitudinal analysis of reproductive skew in male rhesus macaquesAnja Widdig, Fred B Bercovitch, Wolf Jürgen Streich, et al.
Biological Chemistry|March 30, 2016
A systematic comparison of two new releases of exome sequencing products: the aim of use determines the choice of productJanine Altmüller, Susanne Motameny, Christian Becker, et al.
Pageof 52