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Thomas Liehr

Showing results (351-360 of 586) with videos related to

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Oncology Reports|December 2, 2014
MLLT10 and IL3 rearrangement together with a complex four-way translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia: A case reportMoneeb A K Othman, Joana B Melo, Isabel M Carreira, et al.
International Journal of Molecular and Cellular Medicine|September 5, 2017
Prenatal Diagnosis of Mosaic Tetrasomy 18p in a Case without Sonographic AbnormalitiesJavad Karimzad Hagh, Thomas Liehr, Hamid Ghaedi, et al.
Journal of Cancer Research and Clinical Oncology|September 25, 2013
Loss of chromosome 4 correlates with better long-term survival and lower relapse rate after R0-resection of colorectal liver metastasesNadine Aust, Silke Schüle, Annelore K Altendorf-Hofmann, et al.
Cells|March 14, 2026
Comprehensive Cytogenetic and Genomic Profiling of the Murine AML12 (Alpha Mouse Liver 12) Hepatocyte Cell LineDarine Y Asar, Stefanie Kankel, Diandra T Keller, et al.
International Journal of Oncology|June 6, 2007
Cytogenetic characterisation and proteomic profiling of the Imatinib-resistant cell line KCL22-RJulia Rosenhahn, Anja Weise, Susanne Michel, et al.
Current Genomics|April 3, 2018
A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular CharacterizationIoannis Papoulidis, Annalisa Vetro, Vassilis Paspaliaris, et al.
Gene|September 24, 2014
Mitotic stability of small supernumerary marker chromosomes depends on their shape and telomeres - a long term in vitro studyShaymaa Subhi Hussein, Katharina Kreskowski, Monika Ziegler, et al.
American Journal of Medical Genetics. Part A|August 15, 2006
Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCRDiana Mitter, Karin Buiting, Ferdinand von Eggeling, et al.
Molecular Cytogenetics|January 9, 2009
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal maleSofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, et al.
Molecular Cytogenetics|November 19, 2008
Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case reportEmmanouil Manolakos, Nadezda Kosyakova, Loreta Thomaidis, et al.
Pageof 59

Showing results (351-360 of 586) with videos related to

Sort By:
Pageof 59
Oncology Reports|December 2, 2014
MLLT10 and IL3 rearrangement together with a complex four-way translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia: A case reportMoneeb A K Othman, Joana B Melo, Isabel M Carreira, et al.
International Journal of Molecular and Cellular Medicine|September 5, 2017
Prenatal Diagnosis of Mosaic Tetrasomy 18p in a Case without Sonographic AbnormalitiesJavad Karimzad Hagh, Thomas Liehr, Hamid Ghaedi, et al.
Journal of Cancer Research and Clinical Oncology|September 25, 2013
Loss of chromosome 4 correlates with better long-term survival and lower relapse rate after R0-resection of colorectal liver metastasesNadine Aust, Silke Schüle, Annelore K Altendorf-Hofmann, et al.
Cells|March 14, 2026
Comprehensive Cytogenetic and Genomic Profiling of the Murine AML12 (Alpha Mouse Liver 12) Hepatocyte Cell LineDarine Y Asar, Stefanie Kankel, Diandra T Keller, et al.
International Journal of Oncology|June 6, 2007
Cytogenetic characterisation and proteomic profiling of the Imatinib-resistant cell line KCL22-RJulia Rosenhahn, Anja Weise, Susanne Michel, et al.
Current Genomics|April 3, 2018
A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular CharacterizationIoannis Papoulidis, Annalisa Vetro, Vassilis Paspaliaris, et al.
Gene|September 24, 2014
Mitotic stability of small supernumerary marker chromosomes depends on their shape and telomeres - a long term in vitro studyShaymaa Subhi Hussein, Katharina Kreskowski, Monika Ziegler, et al.
American Journal of Medical Genetics. Part A|August 15, 2006
Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCRDiana Mitter, Karin Buiting, Ferdinand von Eggeling, et al.
Molecular Cytogenetics|January 9, 2009
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal maleSofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, et al.
Molecular Cytogenetics|November 19, 2008
Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case reportEmmanouil Manolakos, Nadezda Kosyakova, Loreta Thomaidis, et al.
Pageof 59