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Anja Weise

Showing results (21-30 of 121) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|September 3, 2010
Characterization of chromosomal rearrangements using multicolor-banding (MCB/m-band)Thomas Liehr, Anja Weise, Sophie Hinreiner, et al.
Molecular Cytogenetics|February 20, 2016
Application of multicolor banding combined with heterochromatic and locus-specific probes identify evolutionary conserved breakpoints in Hylobates pileatusWiwat Sangpakdee, Alongklod Tanomtong, Xiaobo Fan, 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.
Journal of Pediatric Surgery|July 10, 2007
t(11;19)(q21;p12~p13.11) and MECT1-MAML2 fusion transcript expression as a prognostic marker in infantile lung mucoepidermoid carcinomaAlexandre Serra, Hans K Schackert, B Mohr, et al.
American Journal of Medical Genetics. Part A|December 8, 2005
Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMCThomas Liehr, Heike Starke, Gabriele Senger, et al.
Molecular Cytogenetics|September 15, 2016
First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the diseaseJelena Filipović, Gordana Joksić, Dragana Vujić, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 30, 2016
A 33-year-old male patient with paternal derived duplication of 14q11.2-14q22.1~22.3: clinical course, phenotypic and genotypic findingsBardo Wannenmacher, Diana Mitter, Franziska Kießling, 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.
International Journal of Oncology|January 1, 2010
New aspects on chromosomal instability: chromosomal break-points in Fanconi anemia patients co-localize on the molecular level with fragile sitesChristiane Schoder, Thomas Liehr, Eunike Velleuer, et al.
Fertility and Sterility|March 4, 2011
Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrierFranck Pellestor, Jacques Puechberty, Anja Weise, et al.
Pageof 13

Showing results (21-30 of 121) with videos related to

Sort By:
Pageof 13
Methods in Molecular Biology (Clifton, N.J.)|September 3, 2010
Characterization of chromosomal rearrangements using multicolor-banding (MCB/m-band)Thomas Liehr, Anja Weise, Sophie Hinreiner, et al.
Molecular Cytogenetics|February 20, 2016
Application of multicolor banding combined with heterochromatic and locus-specific probes identify evolutionary conserved breakpoints in Hylobates pileatusWiwat Sangpakdee, Alongklod Tanomtong, Xiaobo Fan, 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.
Journal of Pediatric Surgery|July 10, 2007
t(11;19)(q21;p12~p13.11) and MECT1-MAML2 fusion transcript expression as a prognostic marker in infantile lung mucoepidermoid carcinomaAlexandre Serra, Hans K Schackert, B Mohr, et al.
American Journal of Medical Genetics. Part A|December 8, 2005
Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMCThomas Liehr, Heike Starke, Gabriele Senger, et al.
Molecular Cytogenetics|September 15, 2016
First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the diseaseJelena Filipović, Gordana Joksić, Dragana Vujić, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 30, 2016
A 33-year-old male patient with paternal derived duplication of 14q11.2-14q22.1~22.3: clinical course, phenotypic and genotypic findingsBardo Wannenmacher, Diana Mitter, Franziska Kießling, 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.
International Journal of Oncology|January 1, 2010
New aspects on chromosomal instability: chromosomal break-points in Fanconi anemia patients co-localize on the molecular level with fragile sitesChristiane Schoder, Thomas Liehr, Eunike Velleuer, et al.
Fertility and Sterility|March 4, 2011
Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrierFranck Pellestor, Jacques Puechberty, Anja Weise, et al.
Pageof 13