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Katharina Wimmer

Showing results (1-10 of 81) with videos related to

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Wiener Medizinische Wochenschrift (1946)|July 23, 2005
[Neurofibromatosis: the most frequent hereditary tumor predisposition syndrome]Katharina Wimmer
Methods in Molecular Biology (Clifton, N.J.)|May 15, 2014
PMS2 gene mutational analysis: direct cDNA sequencing to circumvent pseudogene interferenceKatharina Wimmer, Annekatrin Wernstedt
Human Genetics|August 19, 2008
Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?Katharina Wimmer, Julia Etzler
Plos Genetics|November 30, 2011
The NF1 gene contains hotspots for L1 endonuclease-dependent de novo insertionKatharina Wimmer, Tom Callens, Annekatrin Wernstedt, et al.
Journal of Neuropathology and Experimental Neurology|October 22, 2002
Mutational and expression analysis of the NF1 gene argues against a role as tumor suppressor in sporadic pilocytic astrocytomasKatharina Wimmer, Markus Eckart, Birgit Meyer-Puttlitz, et al.
Genes, Chromosomes & Cancer|June 1, 2006
GAB2 is a novel target of 11q amplification in AML/MDSAndrea Zatkova, Claudia Schoch, Frank Speleman, et al.
European Journal of Human Genetics : EJHG|June 23, 2016
PMS2 inactivation by a complex rearrangement involving an HERV retroelement and the inverted 100-kb duplicon on 7p22.1Julia Vogt, Annekatrin Wernstedt, Tim Ripperger, et al.
European Journal of Human Genetics : EJHG|March 3, 2026
Reporting practices for secondary findings among ERN GENTURIS member institutions in 15 European countriesKathrin Taxer, Katharina Wimmer, Karin Wadt, et al.
Journal of Child Neurology|June 26, 2003
Neurofibromatosis 1: a novel NF1 mutation in an 11-year-old girl with a giant cell granulomaUta Krammer, Katharina Wimmer, Peter Wiesbauer, et al.
Human Mutation|July 4, 2012
Review and update of SPRED1 mutations causing Legius syndromeHilde Brems, Eric Pasmant, Rick Van Minkelen, et al.
Pageof 9

Showing results (1-10 of 81) with videos related to

Sort By:
Pageof 9
Wiener Medizinische Wochenschrift (1946)|July 23, 2005
[Neurofibromatosis: the most frequent hereditary tumor predisposition syndrome]Katharina Wimmer
Methods in Molecular Biology (Clifton, N.J.)|May 15, 2014
PMS2 gene mutational analysis: direct cDNA sequencing to circumvent pseudogene interferenceKatharina Wimmer, Annekatrin Wernstedt
Human Genetics|August 19, 2008
Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?Katharina Wimmer, Julia Etzler
Plos Genetics|November 30, 2011
The NF1 gene contains hotspots for L1 endonuclease-dependent de novo insertionKatharina Wimmer, Tom Callens, Annekatrin Wernstedt, et al.
Journal of Neuropathology and Experimental Neurology|October 22, 2002
Mutational and expression analysis of the NF1 gene argues against a role as tumor suppressor in sporadic pilocytic astrocytomasKatharina Wimmer, Markus Eckart, Birgit Meyer-Puttlitz, et al.
Genes, Chromosomes & Cancer|June 1, 2006
GAB2 is a novel target of 11q amplification in AML/MDSAndrea Zatkova, Claudia Schoch, Frank Speleman, et al.
European Journal of Human Genetics : EJHG|June 23, 2016
PMS2 inactivation by a complex rearrangement involving an HERV retroelement and the inverted 100-kb duplicon on 7p22.1Julia Vogt, Annekatrin Wernstedt, Tim Ripperger, et al.
European Journal of Human Genetics : EJHG|March 3, 2026
Reporting practices for secondary findings among ERN GENTURIS member institutions in 15 European countriesKathrin Taxer, Katharina Wimmer, Karin Wadt, et al.
Journal of Child Neurology|June 26, 2003
Neurofibromatosis 1: a novel NF1 mutation in an 11-year-old girl with a giant cell granulomaUta Krammer, Katharina Wimmer, Peter Wiesbauer, et al.
Human Mutation|July 4, 2012
Review and update of SPRED1 mutations causing Legius syndromeHilde Brems, Eric Pasmant, Rick Van Minkelen, et al.
Pageof 9