Dissecting the genotype in syndromic intellectual disability using whole exome sequencing in addition to genome-wide copy number analysis
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F. Schacherer | D. Haffner | H. Engels | S. Tierling | C. Classen | R. Weber | Anne Kosfeld | V. Riehmer | M. Zivicnjak | C. Landwehr | Sarah Kabisch | S. Heilmann | C. Scholz
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