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Liehr

Showing results (721-730 of 1,099) with videos related to

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Experimental and Therapeutic Medicine|April 25, 2024
An asymptomatic male individual carrying a 5.72 Mb <i>de novo</i> deletion in 8p23.2‑p23.3: A case reportChristina Keramida, Ioannis Papoulidis, Efterpi Pappa, et al.
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.
Acta Physiologica (Oxford, England)|August 4, 2015
Mouse white adipose tissue-derived mesenchymal stem cells gain pericentral and periportal hepatocyte features after differentiation in vitro, which are preserved in vivo after hepatic transplantationS Winkler, M Hempel, S Brückner, et al.
Journal of Agricultural and Food Chemistry|January 24, 2017
Detection of Free Advanced Glycation End Products in Vivo during HemodialysisChristoph Hohmann, Kristin Liehr, Christian Henning, 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.
Cytogenetic and Genome Research|February 14, 2003
A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosisR Trappe, D Böhm, J Kohlhase, 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.
Pageof 110

Showing results (721-730 of 1,099) with videos related to

Sort By:
Pageof 110
Experimental and Therapeutic Medicine|April 25, 2024
An asymptomatic male individual carrying a 5.72 Mb <i>de novo</i> deletion in 8p23.2‑p23.3: A case reportChristina Keramida, Ioannis Papoulidis, Efterpi Pappa, et al.
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.
Acta Physiologica (Oxford, England)|August 4, 2015
Mouse white adipose tissue-derived mesenchymal stem cells gain pericentral and periportal hepatocyte features after differentiation in vitro, which are preserved in vivo after hepatic transplantationS Winkler, M Hempel, S Brückner, et al.
Journal of Agricultural and Food Chemistry|January 24, 2017
Detection of Free Advanced Glycation End Products in Vivo during HemodialysisChristoph Hohmann, Kristin Liehr, Christian Henning, 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.
Cytogenetic and Genome Research|February 14, 2003
A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosisR Trappe, D Böhm, J Kohlhase, 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.
Pageof 110