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Elisabeth Ewers

Showing results (1-10 of 18) with videos related to

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Expert Opinion on Medical Diagnostics|March 15, 2013
Diagnostic applications of fluorescence in situ hybridizationAnja Weise, Kristin Mrasek, Elisabeth Ewers, 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.
Expert Review of Molecular Diagnostics|May 14, 2009
Handling small supernumerary marker chromosomes in prenatal diagnosticsThomas Liehr, Elisabeth Ewers, Nadezda Kosyakova, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|June 16, 2011
Small supernumerary marker chromosomes and uniparental disomy have a story to tellThomas Liehr, Elisabeth Ewers, Ahmed B Hamid, et al.
Current Genomics|March 2, 2011
Somatic mosaicism in cases with small supernumerary marker chromosomesThomas Liehr, Tatyana Karamysheva, Martina Merkas, 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.
Journal of Medical Case Reports|August 5, 2010
Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case reportJoaquín Fernández-Toral, Laura Rodríguez, Ana Plasencia, et al.
American Journal of Medical Genetics. Part A|November 19, 2009
Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsyYasemin Soysal, Sevim Balci, Kuyaş Hekimler, et al.
Molecular Cytogenetics|January 9, 2009
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal maleSofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, et al.
Molecular Cytogenetics|November 14, 2009
A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case reportFrenny Sheth, Elisabeth Ewers, Nadezda Kosyakova, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Expert Opinion on Medical Diagnostics|March 15, 2013
Diagnostic applications of fluorescence in situ hybridizationAnja Weise, Kristin Mrasek, Elisabeth Ewers, 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.
Expert Review of Molecular Diagnostics|May 14, 2009
Handling small supernumerary marker chromosomes in prenatal diagnosticsThomas Liehr, Elisabeth Ewers, Nadezda Kosyakova, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|June 16, 2011
Small supernumerary marker chromosomes and uniparental disomy have a story to tellThomas Liehr, Elisabeth Ewers, Ahmed B Hamid, et al.
Current Genomics|March 2, 2011
Somatic mosaicism in cases with small supernumerary marker chromosomesThomas Liehr, Tatyana Karamysheva, Martina Merkas, 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.
Journal of Medical Case Reports|August 5, 2010
Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case reportJoaquín Fernández-Toral, Laura Rodríguez, Ana Plasencia, et al.
American Journal of Medical Genetics. Part A|November 19, 2009
Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsyYasemin Soysal, Sevim Balci, Kuyaş Hekimler, et al.
Molecular Cytogenetics|January 9, 2009
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal maleSofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, et al.
Molecular Cytogenetics|November 14, 2009
A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case reportFrenny Sheth, Elisabeth Ewers, Nadezda Kosyakova, et al.
Pageof 2