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    Garavelli, L. et al. (n.d.). Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC‐C loci. American journal of medical genetics. 161 (11), pp. 2894-2901. [Online]. 
  
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