A novel de novo paracentric inversion [inv(20)(q13.1q13.3)] accompanied by an 11q14.3-q21 microdeletion in a pediatric patient with an intellectual disability

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Open Access

|Dec 2018

Authors

Genesis Genoma Lab, Genetic Diagnosis, Clinical Genetics & Research, Athens, Greece

Laboratory of Health Physics, Radiobiology & Cytogenetics, NCSR “Demokritos”, Athens, Greece

Genesis Genoma Lab, Genetic Diagnosis, Clinical Genetics & Research, Athens, Greece

Genesis Genoma Lab, Genetic Diagnosis, Clinical Genetics & Research, Athens, Greece

Department of Medical Genetics, Medical School, University of Athens, Athens, Greece

Genesis Genoma Lab, Genetic Diagnosis, Clinical Genetics & Research, Athens, Greece

Genesis Genoma Lab, Genetic Diagnosis, Clinical Genetics & Research, Athens, Greece

Genesis Genoma Lab, Genetic Diagnosis, Clinical Genetics & Research, Athens, Greece

Department of Medical Genetics, Medical School, University of Athens, Athens, Greece

Laboratory of Health Physics, Radiobiology & Cytogenetics, NCSR “Demokritos”, Athens, Greece

Language: English

Page range: 63 - 67

Published on: Dec 31, 2018

In partnership with: Paradigm Publishing Services

Publication frequency: 2 issues per year

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© 2018 S Zachaki, E Kouvidi, A Mitrakos, L Lazaros, A Pantou, A Mavrou, M Tzetis, KN Manola, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.