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Peter Nürnberg

Showing results (1-10 of 517) with videos related to

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Genomics|January 17, 2016
A genomic view on epilepsy and autism candidate genesKamel Jabbari, Peter Nürnberg
Bioinformatics (Oxford, England)|January 14, 2005
ALOHOMORA: a tool for linkage analysis using 10K SNP array dataFranz Rüschendorf, Peter Nürnberg
Bioinformatics (Oxford, England)|September 21, 2004
HaploPainter: a tool for drawing pedigrees with complex haplotypesHolger Thiele, Peter Nürnberg
European Journal of Human Genetics : EJHG|February 2, 2017
Securing the use of existing sample collections for future human genetic researchGeorge Kanoungi, Peter Nürnberg, Michael Nothnagel
Biological Chemistry|September 10, 2013
Enrichment of target sequences for next-generation sequencing applications in research and diagnosticsJanine Altmüller, Birgit S Budde, Peter Nürnberg
Genes|April 9, 2014
Next Generation Sequencing of miRNAs - Strategies, Resources and MethodsSusanne Motameny, Stefanie Wolters, Peter Nürnberg, et al.
Nucleic Acids Research|May 26, 2009
HomozygosityMapper--an interactive approach to homozygosity mappingDominik Seelow, Markus Schuelke, Friedhelm Hildebrandt, et al.
Human Mutation|December 18, 2004
The mutational spectrum of ENPP1 as arising after the analysis of 23 unrelated patients with generalized arterial calcification of infancy (GACI)Nico Ruf, Birgit Uhlenberg, Robert Terkeltaub, et al.
Epilepsy Research|June 7, 2002
Failure to replicate an allelic association between an exon 8 polymorphism of the human alpha(1A) calcium channel gene and common syndromes of idiopathic generalized epilepsyThomas Sander, Mohammad R Toliat, Armin Heils, et al.
Electrophoresis|December 14, 2002
Evaluation of a potential epigenetic biomarker by quantitative methyl-single nucleotide polymorphism analysisKaren Uhlmann, Anja Brinckmann, Mohammad R Toliat, et al.
Pageof 52

Showing results (1-10 of 517) with videos related to

Sort By:
Pageof 52
Genomics|January 17, 2016
A genomic view on epilepsy and autism candidate genesKamel Jabbari, Peter Nürnberg
Bioinformatics (Oxford, England)|January 14, 2005
ALOHOMORA: a tool for linkage analysis using 10K SNP array dataFranz Rüschendorf, Peter Nürnberg
Bioinformatics (Oxford, England)|September 21, 2004
HaploPainter: a tool for drawing pedigrees with complex haplotypesHolger Thiele, Peter Nürnberg
European Journal of Human Genetics : EJHG|February 2, 2017
Securing the use of existing sample collections for future human genetic researchGeorge Kanoungi, Peter Nürnberg, Michael Nothnagel
Biological Chemistry|September 10, 2013
Enrichment of target sequences for next-generation sequencing applications in research and diagnosticsJanine Altmüller, Birgit S Budde, Peter Nürnberg
Genes|April 9, 2014
Next Generation Sequencing of miRNAs - Strategies, Resources and MethodsSusanne Motameny, Stefanie Wolters, Peter Nürnberg, et al.
Nucleic Acids Research|May 26, 2009
HomozygosityMapper--an interactive approach to homozygosity mappingDominik Seelow, Markus Schuelke, Friedhelm Hildebrandt, et al.
Human Mutation|December 18, 2004
The mutational spectrum of ENPP1 as arising after the analysis of 23 unrelated patients with generalized arterial calcification of infancy (GACI)Nico Ruf, Birgit Uhlenberg, Robert Terkeltaub, et al.
Epilepsy Research|June 7, 2002
Failure to replicate an allelic association between an exon 8 polymorphism of the human alpha(1A) calcium channel gene and common syndromes of idiopathic generalized epilepsyThomas Sander, Mohammad R Toliat, Armin Heils, et al.
Electrophoresis|December 14, 2002
Evaluation of a potential epigenetic biomarker by quantitative methyl-single nucleotide polymorphism analysisKaren Uhlmann, Anja Brinckmann, Mohammad R Toliat, et al.
Pageof 52