Cite
HARVARD Citation
Rasmussen, M. et al. (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), pp. 3191-3195. [Online].
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Rasmussen, M. et al. (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), pp. 3191-3195. [Online].