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Thomas Liehr

Showing results (451-460 of 586) with videos related to

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Blood Cells, Molecules & Diseases|January 21, 2014
A yet unreported der(11)t(6;11)(p21;q21) included in a complex karyotype of a refractory anemia with ring sideroblasts and poor prognosisDaiane Correa de Souza, Amanda Faria de Figueiredo, Hasmik Mkrtchyan, et al.
Molecular Syndromology|March 22, 2016
Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II ErrorsRon Hochstenbach, Beata Nowakowska, Marianne Volleth, et al.
Oncology Letters|March 29, 2020
Complex karyotype with cryptic <i>FUS</i> gene rearrangement and deletion of <i>NR3C1</i> and <i>VPREB1</i> genes in childhood B-cell acute lymphoblastic leukemia: A case reportMoneeb A K Othman, Marina Đurišić, Gordana Samardzija, et al.
International Archives of Occupational and Environmental Health|July 15, 2021
Correction to: The association of three DNA repair genes polymorphisms on the frequency of chromosomal alterations detected by fluorescence in situ hybridizationFábio Santiago, Rafaele Tavares Silvestre, Ubirani Barros Otero, et al.
Molecular Syndromology|May 8, 2026
Cytomolecular Analysis of a Ring X Chromosome in a Patient with Turner Syndrome: A Case ReportEvellyn Karine Cruz da Silva, Ruan Barboza Rocha, Paloma de Sousa Passos, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 21, 2010
CD8 locus nuclear dynamics during thymocyte developmentEleni Ktistaki, Anna Garefalaki, Adam Williams, et al.
Cancer Genetics and Cytogenetics|July 13, 2010
Complex karyotype defined by molecular cytogenetic FISH and M-FISH in an infant with acute megakaryoblastic leukemia and neurofibromatosisTerezinha de Jesus Marques-Salles, Hasmik Mkrtchyan, Edinalva Pereira Leite, et al.
Cancer Genetics and Cytogenetics|January 20, 2010
A case of aggressive medulloblastoma with multiple recurrent chromosomal alterationsFabio E da Silva, Ana B Cordeiro, Cleusa Y Nagamachi, et al.
Molecular Cytogenetics|June 20, 2008
Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literatureSvetlana G Vorsanova, Ivan Y Iourov, Victoria Y Voinova-Ulas, et al.
Frontiers in Genetics|August 14, 2023
Turnover of multiple sex chromosomes in <i>Harttia</i> catfish (Siluriformes, Loricariidae): a glimpse from whole chromosome paintingFrancisco de Menezes Cavalcante Sassi, Geize Aparecida Deon, Alexandr Sember, et al.
Pageof 59

Showing results (451-460 of 586) with videos related to

Sort By:
Pageof 59
Blood Cells, Molecules & Diseases|January 21, 2014
A yet unreported der(11)t(6;11)(p21;q21) included in a complex karyotype of a refractory anemia with ring sideroblasts and poor prognosisDaiane Correa de Souza, Amanda Faria de Figueiredo, Hasmik Mkrtchyan, et al.
Molecular Syndromology|March 22, 2016
Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II ErrorsRon Hochstenbach, Beata Nowakowska, Marianne Volleth, et al.
Oncology Letters|March 29, 2020
Complex karyotype with cryptic <i>FUS</i> gene rearrangement and deletion of <i>NR3C1</i> and <i>VPREB1</i> genes in childhood B-cell acute lymphoblastic leukemia: A case reportMoneeb A K Othman, Marina Đurišić, Gordana Samardzija, et al.
International Archives of Occupational and Environmental Health|July 15, 2021
Correction to: The association of three DNA repair genes polymorphisms on the frequency of chromosomal alterations detected by fluorescence in situ hybridizationFábio Santiago, Rafaele Tavares Silvestre, Ubirani Barros Otero, et al.
Molecular Syndromology|May 8, 2026
Cytomolecular Analysis of a Ring X Chromosome in a Patient with Turner Syndrome: A Case ReportEvellyn Karine Cruz da Silva, Ruan Barboza Rocha, Paloma de Sousa Passos, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 21, 2010
CD8 locus nuclear dynamics during thymocyte developmentEleni Ktistaki, Anna Garefalaki, Adam Williams, et al.
Cancer Genetics and Cytogenetics|July 13, 2010
Complex karyotype defined by molecular cytogenetic FISH and M-FISH in an infant with acute megakaryoblastic leukemia and neurofibromatosisTerezinha de Jesus Marques-Salles, Hasmik Mkrtchyan, Edinalva Pereira Leite, et al.
Cancer Genetics and Cytogenetics|January 20, 2010
A case of aggressive medulloblastoma with multiple recurrent chromosomal alterationsFabio E da Silva, Ana B Cordeiro, Cleusa Y Nagamachi, et al.
Molecular Cytogenetics|June 20, 2008
Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literatureSvetlana G Vorsanova, Ivan Y Iourov, Victoria Y Voinova-Ulas, et al.
Frontiers in Genetics|August 14, 2023
Turnover of multiple sex chromosomes in <i>Harttia</i> catfish (Siluriformes, Loricariidae): a glimpse from whole chromosome paintingFrancisco de Menezes Cavalcante Sassi, Geize Aparecida Deon, Alexandr Sember, et al.
Pageof 59