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Thomas Liehr

Showing results (291-300 of 586) with videos related to

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Molecular Cytogenetics|July 2, 2009
Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case reportDilek Aktas, Anja Weise, Eda Utine, et al.
Current Genomics|March 2, 2011
Somatic mosaicism in cases with small supernumerary marker chromosomesThomas Liehr, Tatyana Karamysheva, Martina Merkas, et al.
Genetica|September 20, 2011
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.
Cytogenetic and Genome Research|November 17, 2020
Low-Level Trisomy 14 Mosaicism: A Carrier of an Isochromosome 14 and a Supernumerary Marker Chromosome 14Voula Velissariou, Francis Sachinidi, Stavroula Christopoulou, et al.
Translational Neuroscience|January 27, 2017
Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the <i>DPYD</i> enigmaLukrecija Brečević, Martina Rinčić, Željka Krsnik, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
First patient with trisomy 21 accompanied by an additional der(4)(:p11 --> q11:) plus partial uniparental disomy 4p15-16Heike Starke, Beate Mitulla, Angela Nietzel, et al.
Chromosoma|April 16, 2016
Integrated gene mapping and synteny studies give insights into the evolution of a sex proto-chromosome in Solea senegalensisSilvia Portela-Bens, Manuel Alejandro Merlo, María Esther Rodríguez, et al.
Meta Gene|January 22, 2015
De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic featuresKonstantinos Varvagiannis, Ioannis Papoulidis, Theodora Koromila, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 18, 2025
Satellite DNA Amplification in Advanced Prostate Cancer Is Largely Independent From Euchromatic and Oncogene AmpliconsAnja Weise, Antonio Augusto Ornellas, Gilda Alves, et al.
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.
Pageof 59

Showing results (291-300 of 586) with videos related to

Sort By:
Pageof 59
Molecular Cytogenetics|July 2, 2009
Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case reportDilek Aktas, Anja Weise, Eda Utine, et al.
Current Genomics|March 2, 2011
Somatic mosaicism in cases with small supernumerary marker chromosomesThomas Liehr, Tatyana Karamysheva, Martina Merkas, et al.
Genetica|September 20, 2011
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.
Cytogenetic and Genome Research|November 17, 2020
Low-Level Trisomy 14 Mosaicism: A Carrier of an Isochromosome 14 and a Supernumerary Marker Chromosome 14Voula Velissariou, Francis Sachinidi, Stavroula Christopoulou, et al.
Translational Neuroscience|January 27, 2017
Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the <i>DPYD</i> enigmaLukrecija Brečević, Martina Rinčić, Željka Krsnik, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
First patient with trisomy 21 accompanied by an additional der(4)(:p11 --> q11:) plus partial uniparental disomy 4p15-16Heike Starke, Beate Mitulla, Angela Nietzel, et al.
Chromosoma|April 16, 2016
Integrated gene mapping and synteny studies give insights into the evolution of a sex proto-chromosome in Solea senegalensisSilvia Portela-Bens, Manuel Alejandro Merlo, María Esther Rodríguez, et al.
Meta Gene|January 22, 2015
De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic featuresKonstantinos Varvagiannis, Ioannis Papoulidis, Theodora Koromila, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 18, 2025
Satellite DNA Amplification in Advanced Prostate Cancer Is Largely Independent From Euchromatic and Oncogene AmpliconsAnja Weise, Antonio Augusto Ornellas, Gilda Alves, et al.
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.
Pageof 59