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
Authors
S Zachaki
Genesis Genoma Lab, Genetic Diagnosis, Clinical Genetics & Research, Athens, Greece
Laboratory of Health Physics, Radiobiology & Cytogenetics, NCSR “Demokritos”, Athens, Greece
E Kouvidi
Genesis Genoma Lab, Genetic Diagnosis, Clinical Genetics & Research, Athens, Greece
A Mitrakos
Genesis Genoma Lab, Genetic Diagnosis, Clinical Genetics & Research, Athens, Greece
Department of Medical Genetics, Medical School, University of Athens, Athens, Greece
L Lazaros
Genesis Genoma Lab, Genetic Diagnosis, Clinical Genetics & Research, Athens, Greece
A Pantou
Genesis Genoma Lab, Genetic Diagnosis, Clinical Genetics & Research, Athens, Greece
A Mavrou
Genesis Genoma Lab, Genetic Diagnosis, Clinical Genetics & Research, Athens, Greece
M Tzetis
Department of Medical Genetics, Medical School, University of Athens, Athens, Greece
KN Manola
Laboratory of Health Physics, Radiobiology & Cytogenetics, NCSR “Demokritos”, Athens, Greece
DOI: https://doi.org/10.2478/bjmg-2018-0016 | Journal eISSN: 2199-5761
Language: English
Page range: 63 - 67
Published on: Dec 31, 2018
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Related subjects:
© 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.