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Frontiers in Genetics|January 4, 2024
Small supernumerary marker chromosomes derived from human chromosome 11Thomas Liehr, Monika Ziegler, Luisa Person, et al.Molecular Cytogenetics|January 7, 2011
New cytogenetically visible copy number variant in region 8q21.2Marina Manvelyan, Friedrich W Cremer, Jeannette Lancé, et al.Journal of the Chinese Medical Association : JCMA|May 12, 2010
Small supernumerary marker chromosomes 1 with a normal phenotypeThomas Liehr, Rolf-Dieter Wegner, Markus Stumm, et al.Molecular Cytogenetics|March 16, 2018
Parental origin of deletions and duplications - about the necessity to check for cryptic inversionsThomas Liehr, Isolde Schreyer, Alma Kuechler, et al.The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|April 19, 2012
A new multicolor fluorescence in situ hybridization probe set directed against human heterochromatin: HCM-FISHMaria Bucksch, Monika Ziegler, Nadezda Kosayakova, et al.Journal of Human Genetics|May 14, 2020
Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European populationCarolina Sismani, Stamatia-Maria Rapti, Pavlina Iliopoulou, et al.Molecular Cytogenetics|November 1, 2013
Complex small supernumerary marker chromosomes - an updateThomas Liehr, Sanja Cirkovic, Tanja Lalic, et al.Cytogenetic and Genome Research|April 10, 2014
Mitotic stability of small supernumerary marker chromosomes: a study based on 93 immortalized cell linesHannes Spittel, Florian Kubek, Katharina Kreskowski, et al.Molecular Cytogenetics|April 4, 2013
Heteromorphic variants of chromosome 9Nadezda Kosyakova, Ani Grigorian, Thomas Liehr, et al.Pageof 3