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Liehr

Showing results (861-870 of 1,099) with videos related to

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Oncology Letters|March 22, 2016
A novel <i>IGH@</i> gene rearrangement associated with <i>CDKN2A</i>/<i>B</i> deletion in young adult B-cell acute lymphoblastic leukemiaMoneeb A K Othman, Beata Grygalewicz, Barbara Pienkowska-Grela, et al.
Genetics and Molecular Research : GMR|January 15, 2013
Numerical aberrations of chromosome 17 and TP53 in brain metastases derived from breast cancerD S Vasconcelos, F P E da Silva, L G Quintana, et al.
Diagnostics (Basel, Switzerland)|May 28, 2022
Endoscopic Imaging Technology TodayAxel Boese, Cora Wex, Roland Croner, et al.
Cytogenetic and Genome Research|April 16, 2014
An interstitial 4q31.21q31.22 microdeletion associated with developmental delay: case report and literature reviewAngeliki-Maria Vlaikou, Emmanouil Manolakos, Dimitrios Noutsopoulos, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 19, 2012
Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?Roberta Santos Guilherme, Elisabeth Klein, Claudia Venner, et al.
Human Genetics|September 10, 1999
Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminomaF von Deimling, J M Scharf, T Liehr, et al.
Communications Biology|September 15, 2021
Identifying the lungs as a susceptible site for allele-specific regulatory changes associated with type 1 diabetes riskDaniel Ho, Denis M Nyaga, William Schierding, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic maleM Codina-Pascual, M Oliver-Bonet, J Navarro, et al.
Molecular Cytogenetics|June 13, 2012
Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case reportMilene Vianna Mulatinho, Cassio Luiz de Carvalho Serao, Fernanda Scalco, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|June 28, 2007
Three unusual but cytogenetically similar cases with up to five different cell lines involving structural and numerical abnormalities of chromosome 18Isabel M Carreira, Alexandra Mascarenhas, Eunice Matoso, et al.
Pageof 110

Showing results (861-870 of 1,099) with videos related to

Sort By:
Pageof 110
Oncology Letters|March 22, 2016
A novel <i>IGH@</i> gene rearrangement associated with <i>CDKN2A</i>/<i>B</i> deletion in young adult B-cell acute lymphoblastic leukemiaMoneeb A K Othman, Beata Grygalewicz, Barbara Pienkowska-Grela, et al.
Genetics and Molecular Research : GMR|January 15, 2013
Numerical aberrations of chromosome 17 and TP53 in brain metastases derived from breast cancerD S Vasconcelos, F P E da Silva, L G Quintana, et al.
Diagnostics (Basel, Switzerland)|May 28, 2022
Endoscopic Imaging Technology TodayAxel Boese, Cora Wex, Roland Croner, et al.
Cytogenetic and Genome Research|April 16, 2014
An interstitial 4q31.21q31.22 microdeletion associated with developmental delay: case report and literature reviewAngeliki-Maria Vlaikou, Emmanouil Manolakos, Dimitrios Noutsopoulos, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 19, 2012
Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?Roberta Santos Guilherme, Elisabeth Klein, Claudia Venner, et al.
Human Genetics|September 10, 1999
Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminomaF von Deimling, J M Scharf, T Liehr, et al.
Communications Biology|September 15, 2021
Identifying the lungs as a susceptible site for allele-specific regulatory changes associated with type 1 diabetes riskDaniel Ho, Denis M Nyaga, William Schierding, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic maleM Codina-Pascual, M Oliver-Bonet, J Navarro, et al.
Molecular Cytogenetics|June 13, 2012
Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case reportMilene Vianna Mulatinho, Cassio Luiz de Carvalho Serao, Fernanda Scalco, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|June 28, 2007
Three unusual but cytogenetically similar cases with up to five different cell lines involving structural and numerical abnormalities of chromosome 18Isabel M Carreira, Alexandra Mascarenhas, Eunice Matoso, et al.
Pageof 110