Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome) von Manolakos, Emmanouil, Orru, Sandro, Neroutsou, Rosita, Kefalas, Konstantinos, Louizou, Eirini, Papoulidis, Ioannis, Thomaidis, Loretta, Peitsidis, Panagiotis, Sotiriou, Sotirios, Kitsos, George, Tsoplou, Panagiota, Petersen, Michael B, Metaxotou, Aikaterini

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Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male von Kitsiou-Tzeli, Sofia, Manolakos, Emmanouil, Lagou, Magdalini, Kontodiou, Maria, Kosyakova, Nadezda, Ewers, Elisabeth, Weise, Anja, Garas, Antonios, Orru, Sandro, Liehr, Thomas, Metaxotou, Aikaterini

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Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male von Kitsiou-Tzeli, Sofia, Manolakos, Emmanouil, Lagou, Magdalini, Anagnostopoulou, Katerina, Kontodiou, Maria, Kosyakova, Nadezda, Ewers, Elisabeth, Weise, Anja, Garas, Antonios, Orru, Sandro, Liehr, Thomas, Metaxotou, Aikaterini

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Erratum to: Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male von Kitsiou-Tzeli, Sofia, Manolakos, Emmanouil, Lagou, Magdalini, Anagnostopoulou, Katerina, Kontodiou, Maria, Kosyakova, Nadezda, Ewers, Elisabeth, Weise, Anja, Garas, Antonios, Orru, Sandro, Liehr, Thomas, Metaxotou, Aikaterini

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Correction: Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male von Kitsiou-Tzeli, Sofia, Manolakos, Emmanouil, Lagou, Magdalini, Anagnostopoulou, Katerina, Kontodiou, Maria, Kosyakova, Nadezda, Ewers, Elisabeth, Weise, Anja, Garas, Antonios, Orru, Sandro, Liehr, Thomas, Metaxotou, Aikaterini

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