The development of four multiplex assays, the two "mini-multiplexes" and the two "midi-multiplexes" described, increased the success rate for the analysis of the entire control region sequences in highly and moderately degraded samples compared to conventional approaches traditionally used for forensic applications (HVS-1/HVS-II). The authors found that these multiplex assays met the demands of routine forensic mtDNA work that dealt with various kinds of biological samples which exhibited varying mtDNA degradation states. Handling the combined application of degradation-sensitive real-time quantitative PCR and the appropriate mtDNA amplification in actual casework samples over time yielded limits of detection that were 300-400 genome equivalents of target mtDNA for the midi-amplicons and 200-300 genome equivalents for the mini-amplicons. The upstream quantitation assay provided useful information for the selection of the appropriate amplification and sequencing strategy. The proposed procedure used a preceding mtDNA quantitation step by real time PCR with two different target fragments (143 and 283 bp) that approximately corresponded to the average fragment sizes of the different multiplex approaches in order to estimate size-dependent mtDNA quantities and to aid the choice of the appropriate PCR multiplexes regarding quality of the results and required costs. Nine evidentiary hair shafts, all between 1.5 and 5 cm in length were subjected to mtDNA analyses. The hair shafts that were longer than 1.5 cm were cut into two equal pieces for independent analysis. The extraction process is described in detail, and an actual case work example that used the proposed method is presented. 3 figures, 3 tables, and 6 references