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APA Citation
Rasmussen, M., Ramsing, M., Petersen, O. B., Vogel, I., & Sunde, L. (n.d.). a description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variability. American journal of medical genetics, 161(12), 3191–3195. http://access.bl.uk/ark:/81055/vdc_100090660939.0x000018