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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.
Experimental and Therapeutic Medicine|March 27, 2014
Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literatureEmmanouil Manolakos, Annalisa Vetro, Antonios Garas, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 29, 2014
Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literatureStavros Sifakis, Makarios Eleftheriades, Dimitra Kappou, et al.
Genes, Chromosomes & Cancer|April 30, 2002
Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemiaIvan F Loncarevic, Jennifer Römer, Heike Starke, et al.
Current Genomics|April 3, 2018
A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular CharacterizationIoannis Papoulidis, Annalisa Vetro, Vassilis Paspaliaris, et al.
Gene|September 24, 2014
Mitotic stability of small supernumerary marker chromosomes depends on their shape and telomeres - a long term in vitro studyShaymaa Subhi Hussein, Katharina Kreskowski, Monika Ziegler, 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.
Oncology Letters|January 23, 2020
Molecular cytogenetic pilot study on pleomorphic adenomas of salivary glandsJovanna Thielker, Anja Weise, Moneeb A K Othman, et al.
Cytogenetic and Genome Research|December 19, 2015
Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning DifficultiesMaria Kontodiou, Georgios Daskalakis, Annalisa Vetro, et al.
Cytogenetic and Genome Research|April 16, 2014
An interstitial 4q31.21q31.22 microdeletion associated with developmental delay: case report and literature reviewAngeliki-Maria Vlaikou, Emmanouil Manolakos, Dimitrios Noutsopoulos, et al.
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