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APA Citation
Riehmer, V., Erger, F., Herkenrath, P., Seland, S., Jackels, M., Wiater, A., Heller, R., Beck, B. B., & Netzer, C. (2017). a heritable microduplication encompassing TBL1XR1 causes a genomic sister‐disorder for the 3q26.32 microdeletion syndrome. American journal of medical genetics, 173(8), 2132–2138. http://access.bl.uk/ark:/81055/vdc_100047735109.0x000034