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2p15-p16.1 microdeletion syndrome
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A patient with de novo 0.45Mb deletion of 2p16.1: The role of BCL11A, PAPOLG, REL, and FLJ16341 in the 2p15-p16.1 microdeletion syndrome
2013 |
Second Faculty of Medicine
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Identification of a patient with intellectual disability and de novo 3.7 Mb deletion supports the existence of a novel microdeletion syndrome in 2p14-p15
2013 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport