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Although MPNST lack a distinctive cytogenetic signature that allows for a specific diagnosis, molecular alterations including EGFR amplification, and deletions of NF1 or CDKN2A ( p16 ) are supportive in the appropriate setting[77, 97, 106, 112]
The percentage difference between calculated and measured LDL-C (total error) and the number of results exceeding the total error goal of 12% were established
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When the record is unclear about the primary site, query the treating physician before assigning either code
