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Thomas Liehr

Showing results (201-210 of 586) with videos related to

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The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 8, 2005
Dup(13)(q14.2-q14.3): yet another new differential diagnostic aspect for short stature-like phenotypeIsolde Schreyer, Annett Neumann, Volkmar Beensen, et al.
Molecular Cytogenetics|December 2, 2014
Comprehensive chronic lymphocytic leukemia diagnostics by combined multiplex ligation dependent probe amplification (MLPA) and interphase fluorescence in situ hybridization (iFISH)Eyad Alhourani, Martina Rincic, Moneeb Ak Othman, et al.
Journal of Prenatal Medicine|July 1, 2016
Alpha-fetoprotein and its value for predicting pregnancy outcomes - a re-evaluationAyham Alhaj Darouich, Thomas Liehr, Anja Weise, et al.
Indian Journal of Human Genetics|February 6, 2014
Chromosomal abnormalities in couples with repeated fetal loss: An Indian retrospective studyFrenny J Sheth, Thomas Liehr, Pritti Kumari, et al.
Molecular Cytogenetics|June 6, 2008
Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among themThomas Liehr, Kristin Mrasek, Nadezda Kosyakova, et al.
Molecular Cytogenetics|March 22, 2021
Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genesEmanuele G Coci, Udo Koehler, Thomas Liehr, et al.
International Journal of Oncology|December 5, 2003
Breakpoint differentiation in chromosomal aberrations of hematological malignancies: Identification of 33 previously unrecorded breakpointsAnita Heller, Ivan F Loncarevic, Melanie Glaser, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|December 20, 2018
Heterochromatic regions in Japanese quail chromosomes: comprehensive molecular-cytogenetic characterization and 3D mapping in interphase nucleusAnna Zlotina, Antonina Maslova, Nadezda Kosyakova, et al.
Frontiers in Genetics|December 5, 2019
Recombinant Chromosomes Resulting From Parental Pericentric Inversions-Two New Cases and a Review of the LiteratureThomas Liehr, Anja Weise, Kristin Mrasek, et al.
Molecular Cytogenetics|September 26, 2014
An adult B-cell precursor acute lymphoblastic leukemia with multiple secondary cytogenetic aberrationsWalid Al-Achkar, Abdulsamad Wafa, Moneeb Abdullah Kassem Othman, et al.
Pageof 59

Showing results (201-210 of 586) with videos related to

Sort By:
Pageof 59
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 8, 2005
Dup(13)(q14.2-q14.3): yet another new differential diagnostic aspect for short stature-like phenotypeIsolde Schreyer, Annett Neumann, Volkmar Beensen, et al.
Molecular Cytogenetics|December 2, 2014
Comprehensive chronic lymphocytic leukemia diagnostics by combined multiplex ligation dependent probe amplification (MLPA) and interphase fluorescence in situ hybridization (iFISH)Eyad Alhourani, Martina Rincic, Moneeb Ak Othman, et al.
Journal of Prenatal Medicine|July 1, 2016
Alpha-fetoprotein and its value for predicting pregnancy outcomes - a re-evaluationAyham Alhaj Darouich, Thomas Liehr, Anja Weise, et al.
Indian Journal of Human Genetics|February 6, 2014
Chromosomal abnormalities in couples with repeated fetal loss: An Indian retrospective studyFrenny J Sheth, Thomas Liehr, Pritti Kumari, et al.
Molecular Cytogenetics|June 6, 2008
Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among themThomas Liehr, Kristin Mrasek, Nadezda Kosyakova, et al.
Molecular Cytogenetics|March 22, 2021
Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genesEmanuele G Coci, Udo Koehler, Thomas Liehr, et al.
International Journal of Oncology|December 5, 2003
Breakpoint differentiation in chromosomal aberrations of hematological malignancies: Identification of 33 previously unrecorded breakpointsAnita Heller, Ivan F Loncarevic, Melanie Glaser, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|December 20, 2018
Heterochromatic regions in Japanese quail chromosomes: comprehensive molecular-cytogenetic characterization and 3D mapping in interphase nucleusAnna Zlotina, Antonina Maslova, Nadezda Kosyakova, et al.
Frontiers in Genetics|December 5, 2019
Recombinant Chromosomes Resulting From Parental Pericentric Inversions-Two New Cases and a Review of the LiteratureThomas Liehr, Anja Weise, Kristin Mrasek, et al.
Molecular Cytogenetics|September 26, 2014
An adult B-cell precursor acute lymphoblastic leukemia with multiple secondary cytogenetic aberrationsWalid Al-Achkar, Abdulsamad Wafa, Moneeb Abdullah Kassem Othman, et al.
Pageof 59