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Taken together with the findings of routine histopathologic examination and IHC, this genomic profile, with mutation in PRKAR1A only and monosomies of multiple chromosomes, including 1, 2, and 17, was diagnostic for MMNSTs

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A case of oxalate nephropathy associated with prolonged cholecystostomy tube placement

49.Hernandez AF, Green JB, Janmohamed S, et al