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K Kutsche

Showing results (1-10 of 20) with videos related to

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Cytogenetics and Cell Genetics|June 14, 2002
The mouse Arhgef6 gene: cDNA sequence, expression analysis, and chromosome assignmentK Kutsche, A Gal
Herz|May 31, 2017
Genetic diagnostics of inherited aortic diseases : Medical strategy analysisY von Kodolitsch, K Kutsche
Methods in Molecular Biology (Clifton, N.J.)|March 23, 2019
Induced Neurons for the Study of Neurodegenerative and Neurodevelopmental DisordersEvelyn J Sauter, Lisa K Kutsche, Simon D Klapper, et al.
Oncogene|November 11, 1999
Predetermined chromosomal deletion encompassing the Nf-1 geneT Schlake, I Schupp, K Kutsche, et al.
Cytogenetic and Genome Research|August 6, 2003
Microphthalmia with linear skin defects syndrome (MLS): a male with a mosaic paracentric inversion of XpK Kutsche, W Werner, O Bartsch, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 18, 2012
Oculo-facio-cardio-dental syndrome in three succeeding generations: genotypic data and phenotypic featuresB Lozić, J Ljubković, D Gabrić Pandurić, et al.
Clinical Genetics|January 29, 2013
Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two lociB Chilian, H Abdollahpour, T Bierhals, et al.
Hormones and Behavior|May 28, 2015
Structure-function-behavior relationship in estrogen-induced synaptic plasticityR Vierk, J Bayer, S Freitag, et al.
Cytogenetic and Genome Research|October 19, 2013
Branchio-otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8T Schmidt, T Bierhals, F Kortüm, et al.
Molecular Syndromology|May 10, 2012
Hallermann-Streiff Syndrome: No Evidence for a Link to LaminopathiesF Kortüm, M Chyrek, S Fuchs, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Cytogenetics and Cell Genetics|June 14, 2002
The mouse Arhgef6 gene: cDNA sequence, expression analysis, and chromosome assignmentK Kutsche, A Gal
Herz|May 31, 2017
Genetic diagnostics of inherited aortic diseases : Medical strategy analysisY von Kodolitsch, K Kutsche
Methods in Molecular Biology (Clifton, N.J.)|March 23, 2019
Induced Neurons for the Study of Neurodegenerative and Neurodevelopmental DisordersEvelyn J Sauter, Lisa K Kutsche, Simon D Klapper, et al.
Oncogene|November 11, 1999
Predetermined chromosomal deletion encompassing the Nf-1 geneT Schlake, I Schupp, K Kutsche, et al.
Cytogenetic and Genome Research|August 6, 2003
Microphthalmia with linear skin defects syndrome (MLS): a male with a mosaic paracentric inversion of XpK Kutsche, W Werner, O Bartsch, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 18, 2012
Oculo-facio-cardio-dental syndrome in three succeeding generations: genotypic data and phenotypic featuresB Lozić, J Ljubković, D Gabrić Pandurić, et al.
Clinical Genetics|January 29, 2013
Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two lociB Chilian, H Abdollahpour, T Bierhals, et al.
Hormones and Behavior|May 28, 2015
Structure-function-behavior relationship in estrogen-induced synaptic plasticityR Vierk, J Bayer, S Freitag, et al.
Cytogenetic and Genome Research|October 19, 2013
Branchio-otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8T Schmidt, T Bierhals, F Kortüm, et al.
Molecular Syndromology|May 10, 2012
Hallermann-Streiff Syndrome: No Evidence for a Link to LaminopathiesF Kortüm, M Chyrek, S Fuchs, et al.
Pageof 2