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Riehmer, V. et al. (2017). A heritable microduplication encompassing TBL1XR1 causes a genomic sister‐disorder for the 3q26.32 microdeletion syndrome. American journal of medical genetics. 173 (8), pp. 2132-2138. [Online].
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Riehmer, V. et al. (2017). A heritable microduplication encompassing TBL1XR1 causes a genomic sister‐disorder for the 3q26.32 microdeletion syndrome. American journal of medical genetics. 173 (8), pp. 2132-2138. [Online].