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Thomas Liehr

Showing results (91-100 of 586) with videos related to

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Expert Review of Molecular Diagnostics|February 10, 2015
The current state of molecular cytogenetics in cancer diagnosisThomas Liehr, Moneeb A K Othman, Katharina Rittscher, et al.
International Journal of Laboratory Hematology|May 9, 2022
Intrachromosomal amplification of BCR expressed as homogenously staining region (hsr) in a case of acute myeloid leukemia with myelodysplasia-related changesPurvi Mohanty, Dhanlaxmi Shetty, Thomas Liehr, et al.
BMC Genomics|February 22, 2016
Microdissection of lampbrush chromosomes as an approach for generation of locus-specific FISH-probes and samples for high-throughput sequencingAnna Zlotina, Tatiana Kulikova, Nadezda Kosyakova, et al.
Genes|November 18, 2017
New Insights into Phasmatodea ChromosomesThomas Liehr, Olesya Buleu, Tatyana Karamysheva, et al.
Fertility and Sterility|March 23, 2015
Meiotic and sperm aneuploidy studies in three carriers of Robertsonian translocations and small supernumerary marker chromosomesGordon Kirkpatrick, He Ren, Thomas Liehr, et al.
Cytogenetic and Genome Research|May 26, 2024
Molecular Cytogenetic Characterization of Rare but Repeatedly Observed Inversions in German PopulationJoana Seixas, Niklas Padutsch, Stefanie Kankel, et al.
Biomedicine Hub|January 29, 2020
Noninvasive Prenatal Testing - When Is It Advantageous to ApplyThomas Liehr, Angela Lauten, Uwe Schneider, et al.
Molecular Cytogenetics|June 23, 2016
Comparative analysis of individual chromosome involvement in micronuclei induced by mitomycin C and bleomycin in human leukocytesGalina Hovhannisyan, Rouben Aroutiounian, Nelly Babayan, et al.
European Journal of Medical Genetics|September 24, 2005
Narrowing the deleted region associated with the 15q21 syndromeTiziano Pramparo, Teresa Mattina, Stefania Gimelli, et al.
Gene|September 4, 2013
Prenatally detected interstitial deletion 13q12.3-q22 in a fetus with a cystic hygromaAna Vičić, Damir Zudenigo, Petra Korać, et al.
Pageof 59

Showing results (91-100 of 586) with videos related to

Sort By:
Pageof 59
Expert Review of Molecular Diagnostics|February 10, 2015
The current state of molecular cytogenetics in cancer diagnosisThomas Liehr, Moneeb A K Othman, Katharina Rittscher, et al.
International Journal of Laboratory Hematology|May 9, 2022
Intrachromosomal amplification of BCR expressed as homogenously staining region (hsr) in a case of acute myeloid leukemia with myelodysplasia-related changesPurvi Mohanty, Dhanlaxmi Shetty, Thomas Liehr, et al.
BMC Genomics|February 22, 2016
Microdissection of lampbrush chromosomes as an approach for generation of locus-specific FISH-probes and samples for high-throughput sequencingAnna Zlotina, Tatiana Kulikova, Nadezda Kosyakova, et al.
Genes|November 18, 2017
New Insights into Phasmatodea ChromosomesThomas Liehr, Olesya Buleu, Tatyana Karamysheva, et al.
Fertility and Sterility|March 23, 2015
Meiotic and sperm aneuploidy studies in three carriers of Robertsonian translocations and small supernumerary marker chromosomesGordon Kirkpatrick, He Ren, Thomas Liehr, et al.
Cytogenetic and Genome Research|May 26, 2024
Molecular Cytogenetic Characterization of Rare but Repeatedly Observed Inversions in German PopulationJoana Seixas, Niklas Padutsch, Stefanie Kankel, et al.
Biomedicine Hub|January 29, 2020
Noninvasive Prenatal Testing - When Is It Advantageous to ApplyThomas Liehr, Angela Lauten, Uwe Schneider, et al.
Molecular Cytogenetics|June 23, 2016
Comparative analysis of individual chromosome involvement in micronuclei induced by mitomycin C and bleomycin in human leukocytesGalina Hovhannisyan, Rouben Aroutiounian, Nelly Babayan, et al.
European Journal of Medical Genetics|September 24, 2005
Narrowing the deleted region associated with the 15q21 syndromeTiziano Pramparo, Teresa Mattina, Stefania Gimelli, et al.
Gene|September 4, 2013
Prenatally detected interstitial deletion 13q12.3-q22 in a fetus with a cystic hygromaAna Vičić, Damir Zudenigo, Petra Korać, et al.
Pageof 59