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. 2018 Apr 16;14(4):e1007355. doi: 10.1371/journal.pgen.1007355

Fig 2. Pedigrees of patients carrying truncating/deleterious mutations in new candidate PrCa risk genes involved in Fanconi anemia.

Fig 2

(A) Patient HPC186 harboring the RAD51C frameshift mutation c.890_899del. (B) Patient HPC447 harboring the FANCD2 splicing mutation c.2494+2T>C. (C) Patient HPC150 harboring the FANCI frameshift mutation c.206del. Electropherograms of the Sanger sequencing validations are shown.