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J Plaschke

Showing results (1-10 of 21) with videos related to

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Journal of Medical Genetics|August 16, 2003
Genomic rearrangements of hMSH6 contribute to the genetic predisposition in suspected hereditary non-polyposis colorectal cancer syndromeJ Plaschke, J Rüschoff, H K Schackert
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|October 31, 2013
Detection of genetic diversity in closely related bread wheat using microsatellite markersJ Plaschke, M W Ganal, M S Röder
Clinical Chemistry and Laboratory Medicine|December 22, 1999
Quantitative differences between aberrant transcripts which occur as common isoforms and due to mutation-based exon skipping of the mismatch repair gene hMLH1J Plaschke, C Bulitta, H D Saeger, et al.
Biotechniques|May 20, 1998
Doublex sequencing in molecular diagnosis of hereditary diseasesJ Plaschke, H Voss, M Hahn, et al.
Journal of Medical Genetics|September 9, 2000
BRCA2 germline mutations among early onset breast cancer patients unselected for family history of the diseaseJ Plaschke, T Commer, C Jacobi, et al.
Journal of Cancer Research and Clinical Oncology|January 27, 2005
Low-level microsatellite instability phenotype in sporadic glioblastoma multiformeR Martinez, H K Schackert, H Appelt, et al.
Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress|October 2, 2003
[Sequence analysis of BRCA1 gene in young breast cancer patients and/or positive family history]M Hampl, J Plaschke, R Burgemeister, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|November 8, 2013
RFLP mapping of genes affecting plant height and growth habit in ryeJ Plaschke, A Börner, D X Xie, et al.
Biochemical and Biophysical Research Communications|August 15, 1998
Evidence that TSG101 aberrant transcripts are PCR artifactsM Hampl, J Hampl, J Plaschke, et al.
Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress|October 2, 2003
[Molecular diagnosis and clinical consequences in families with HNPCC syndrome]S Pistorius, J Plaschke, C Kruppa, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|August 16, 2003
Genomic rearrangements of hMSH6 contribute to the genetic predisposition in suspected hereditary non-polyposis colorectal cancer syndromeJ Plaschke, J Rüschoff, H K Schackert
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|October 31, 2013
Detection of genetic diversity in closely related bread wheat using microsatellite markersJ Plaschke, M W Ganal, M S Röder
Clinical Chemistry and Laboratory Medicine|December 22, 1999
Quantitative differences between aberrant transcripts which occur as common isoforms and due to mutation-based exon skipping of the mismatch repair gene hMLH1J Plaschke, C Bulitta, H D Saeger, et al.
Biotechniques|May 20, 1998
Doublex sequencing in molecular diagnosis of hereditary diseasesJ Plaschke, H Voss, M Hahn, et al.
Journal of Medical Genetics|September 9, 2000
BRCA2 germline mutations among early onset breast cancer patients unselected for family history of the diseaseJ Plaschke, T Commer, C Jacobi, et al.
Journal of Cancer Research and Clinical Oncology|January 27, 2005
Low-level microsatellite instability phenotype in sporadic glioblastoma multiformeR Martinez, H K Schackert, H Appelt, et al.
Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress|October 2, 2003
[Sequence analysis of BRCA1 gene in young breast cancer patients and/or positive family history]M Hampl, J Plaschke, R Burgemeister, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|November 8, 2013
RFLP mapping of genes affecting plant height and growth habit in ryeJ Plaschke, A Börner, D X Xie, et al.
Biochemical and Biophysical Research Communications|August 15, 1998
Evidence that TSG101 aberrant transcripts are PCR artifactsM Hampl, J Hampl, J Plaschke, et al.
Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress|October 2, 2003
[Molecular diagnosis and clinical consequences in families with HNPCC syndrome]S Pistorius, J Plaschke, C Kruppa, et al.
Pageof 3