A de novo non-sense mutation in ZBTB18 in a patient with features of the 1q43q44 microdeletion syndrome

Overview of attention for article published in European Journal of Human Genetics, November 2013

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A de novo non-sense mutation in ZBTB18 in a patient with features of the 1q43q44 microdeletion syndrome. http://t.co/CiZiqG3i3t @knoers

#ZBTB18 de novo mutation mimicks the 1q43q44 phenotype http://t.co/esRz66axFJ

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