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Thomas Liehr

Showing results (301-310 of 586) with videos related to

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Archivos Argentinos De Pediatria|January 28, 2020
Algorithm for the diagnosis of patients with neurodevelopmental disorders and suspicion of a genetic syndromeLuis A Méndez-Rosado, Damaris García, Odalis Molina-Gamboa, et al.
Genetica|December 21, 2017
Correction to: Whole chromosome painting reveals independent origin of sex chromosomes in closely related forms of a fish speciesMarcelo de Bello Cioffi, Antonio Sánchez, Juan Alberto Marchal, et al.
Journal of Assisted Reproduction and Genetics|January 24, 2018
Characterization of a complex chromosomal rearrangement involving chromosomes 1, 3, and 4 in a slightly affected male with bad obstetrics historyPritti K Priya, Vineet V Mishra, Thomas Liehr, et al.
European Journal of Medical Genetics|May 31, 2011
Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case reportLilia Kraoua, Myriam Chaabouni, Elisabeth Ewers, et al.
BMC Hematology|September 7, 2018
A new adult AML case with an extremely complex karyotype, remission and relapse combined with high hyperdiploidy of a normal chromosome set in secondary AMLAbdulsamad Wafa, Suher ALmedania, Abdulmunim Aljapawe, et al.
Journal of Experimental Zoology. Part B, Molecular and Developmental Evolution|February 26, 2024
Variants of a major DNA satellite discriminate parental subgenomes in a hybrid parthenogenetic lizard Darevskia unisexualis (Darevsky, 1966)Pavel Nikitin, Sviatoslav Sidorov, Thomas Liehr, et al.
Prenatal Diagnosis|September 17, 2003
First postnatal case of mosaic del(22)/r(22)Heike Starke, Beate Mitulla, Volkmar Beensen, et al.
Leukemia Research and Treatment|November 7, 2014
A Novel Cryptic Three-Way Translocation t(2;9;18)(p23.2;p21.3;q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic LeukemiaMoneeb A K Othman, Martina Rincic, Joana B Melo, et al.
Expert Review of Molecular Diagnostics|April 11, 2013
Multicolor FISH methods in current clinical diagnosticsThomas Liehr, Anja Weise, Ahmed B Hamid, et al.
Genome|July 22, 2017
Spatial organization of fibroblast and spermatocyte nuclei with different B-chromosome content in Korean field mouse, Apodemus peninsulae (Rodentia, Muridae)Tatyana V Karamysheva, Anna A Torgasheva, Yaroslav R Yefremov, et al.
Pageof 59

Showing results (301-310 of 586) with videos related to

Sort By:
Pageof 59
Archivos Argentinos De Pediatria|January 28, 2020
Algorithm for the diagnosis of patients with neurodevelopmental disorders and suspicion of a genetic syndromeLuis A Méndez-Rosado, Damaris García, Odalis Molina-Gamboa, et al.
Genetica|December 21, 2017
Correction to: Whole chromosome painting reveals independent origin of sex chromosomes in closely related forms of a fish speciesMarcelo de Bello Cioffi, Antonio Sánchez, Juan Alberto Marchal, et al.
Journal of Assisted Reproduction and Genetics|January 24, 2018
Characterization of a complex chromosomal rearrangement involving chromosomes 1, 3, and 4 in a slightly affected male with bad obstetrics historyPritti K Priya, Vineet V Mishra, Thomas Liehr, et al.
European Journal of Medical Genetics|May 31, 2011
Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case reportLilia Kraoua, Myriam Chaabouni, Elisabeth Ewers, et al.
BMC Hematology|September 7, 2018
A new adult AML case with an extremely complex karyotype, remission and relapse combined with high hyperdiploidy of a normal chromosome set in secondary AMLAbdulsamad Wafa, Suher ALmedania, Abdulmunim Aljapawe, et al.
Journal of Experimental Zoology. Part B, Molecular and Developmental Evolution|February 26, 2024
Variants of a major DNA satellite discriminate parental subgenomes in a hybrid parthenogenetic lizard Darevskia unisexualis (Darevsky, 1966)Pavel Nikitin, Sviatoslav Sidorov, Thomas Liehr, et al.
Prenatal Diagnosis|September 17, 2003
First postnatal case of mosaic del(22)/r(22)Heike Starke, Beate Mitulla, Volkmar Beensen, et al.
Leukemia Research and Treatment|November 7, 2014
A Novel Cryptic Three-Way Translocation t(2;9;18)(p23.2;p21.3;q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic LeukemiaMoneeb A K Othman, Martina Rincic, Joana B Melo, et al.
Expert Review of Molecular Diagnostics|April 11, 2013
Multicolor FISH methods in current clinical diagnosticsThomas Liehr, Anja Weise, Ahmed B Hamid, et al.
Genome|July 22, 2017
Spatial organization of fibroblast and spermatocyte nuclei with different B-chromosome content in Korean field mouse, Apodemus peninsulae (Rodentia, Muridae)Tatyana V Karamysheva, Anna A Torgasheva, Yaroslav R Yefremov, et al.
Pageof 59