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Thomas Liehr

Showing results (141-150 of 586) with videos related to

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Molecular Cytogenetics|March 23, 2018
Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44)Faten Moassass, Abdulsamad Wafa, Thomas Liehr, et al.
Clinical Dysmorphology|May 9, 2018
De-novo interstitial 2.33 Mb deletion in 8q24.3: new insights on a very rare partial monosomy syndromeSusan Akbaroghli, Seyed H Tonekaboni, Roxana Kariminejad, et al.
Cytogenetic and Genome Research|March 23, 2020
Application of Tris-HCl Allows the Specific Labeling of Regularly Prepared Chromosomes by CRISPR-FISHBhanu P Potlapalli, Veit Schubert, Janina Metje-Sprink, et al.
Genes|April 30, 2021
Comparative Distribution of Repetitive Sequences in the Karyotypes of <i>Xenopus tropicalis</i> and <i>Xenopus laevis</i> (Anura, Pipidae)Álvaro S Roco, Thomas Liehr, Adrián Ruiz-García, et al.
Cells|November 27, 2024
Cytogenomic Characterization of Murine Neuroblastoma Cell Line Neuro-2a and Its Two Derivatives Neuro-2a TR-Alpha and Neuro-2a TR-BetaLioba Hergenhahn, Niklas Padutsch, Shaymaa Azawi, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|June 23, 2010
Centromere activity in dicentric small supernumerary marker chromosomesElisabeth Ewers, Kinya Yoda, Ahmed B Hamid, et al.
Genes|August 28, 2025
Customized Chromosomal Microarrays for Neurodevelopmental DisordersMartina Rincic, Lukrecija Brecevic, Thomas Liehr, et al.
European Journal of Medical Genetics|December 19, 2006
An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotypeIris Bartels, Heike Starke, Loukas Argyriou, et al.
Journal of Pediatric Surgery|July 10, 2007
t(11;19)(q21;p12~p13.11) and MECT1-MAML2 fusion transcript expression as a prognostic marker in infantile lung mucoepidermoid carcinomaAlexandre Serra, Hans K Schackert, B Mohr, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|April 12, 2011
Normal prenatal ultrasound findings in a case with de novo mosaic small supernumerary marker chromosome 18--how to counsel?Christel Eckmann-Scholz, Holger Tönnies, Thomas Liehr, et al.
Pageof 59

Showing results (141-150 of 586) with videos related to

Sort By:
Pageof 59
Molecular Cytogenetics|March 23, 2018
Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44)Faten Moassass, Abdulsamad Wafa, Thomas Liehr, et al.
Clinical Dysmorphology|May 9, 2018
De-novo interstitial 2.33 Mb deletion in 8q24.3: new insights on a very rare partial monosomy syndromeSusan Akbaroghli, Seyed H Tonekaboni, Roxana Kariminejad, et al.
Cytogenetic and Genome Research|March 23, 2020
Application of Tris-HCl Allows the Specific Labeling of Regularly Prepared Chromosomes by CRISPR-FISHBhanu P Potlapalli, Veit Schubert, Janina Metje-Sprink, et al.
Genes|April 30, 2021
Comparative Distribution of Repetitive Sequences in the Karyotypes of <i>Xenopus tropicalis</i> and <i>Xenopus laevis</i> (Anura, Pipidae)Álvaro S Roco, Thomas Liehr, Adrián Ruiz-García, et al.
Cells|November 27, 2024
Cytogenomic Characterization of Murine Neuroblastoma Cell Line Neuro-2a and Its Two Derivatives Neuro-2a TR-Alpha and Neuro-2a TR-BetaLioba Hergenhahn, Niklas Padutsch, Shaymaa Azawi, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|June 23, 2010
Centromere activity in dicentric small supernumerary marker chromosomesElisabeth Ewers, Kinya Yoda, Ahmed B Hamid, et al.
Genes|August 28, 2025
Customized Chromosomal Microarrays for Neurodevelopmental DisordersMartina Rincic, Lukrecija Brecevic, Thomas Liehr, et al.
European Journal of Medical Genetics|December 19, 2006
An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotypeIris Bartels, Heike Starke, Loukas Argyriou, et al.
Journal of Pediatric Surgery|July 10, 2007
t(11;19)(q21;p12~p13.11) and MECT1-MAML2 fusion transcript expression as a prognostic marker in infantile lung mucoepidermoid carcinomaAlexandre Serra, Hans K Schackert, B Mohr, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|April 12, 2011
Normal prenatal ultrasound findings in a case with de novo mosaic small supernumerary marker chromosome 18--how to counsel?Christel Eckmann-Scholz, Holger Tönnies, Thomas Liehr, et al.
Pageof 59