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Linkage analysis studies have identified two CNC genetic loci: (1) a 6.4-cM region on chromosome 2 (2p16) and (2) a 17-cM region on chromosome 17 (17]22-24) [6, 7].
However, none of our QTLs are localized at 34 cM region.
Using a genetic cross with Azucena, we mapped Bsdr1 onto a 30.8 cM region on chromosome 12.
Our previous study showed that the HWC2 locus was located within the 3.9-cM region between two RFLP markers: XNpb264 and XNpb197.
Additionally, the QTL qCTB-7 mapped to a 6.8-cM region near RM11-RM2752 on rice chromosome 7 (Lin et al. [2010]).
Most of the pelotons were observed in the apex of the roots, in the 1 5 cm region from the tip (Table 1).
A major QTL, designated qPbm11, was identified in the 30.8 cM region between markers aa11000537 and aa11001573 on chromosome 11, with a contribution of 30.8% to the phenotype.
SUB1 was further mapped with circa 3,000 F2 progeny to a 0.16-cM region on chromosome 9 (Xu et al., 2000).
Paraffin wax heated up to above 60 °C was used as paint to cover 3/4 of the sample region, exposing the rest 1 cm × 1 cm region to the electrolyte for anodization.
A 10 cM region around the test location was excluded for selection of the five control markers.
The gene was primo-localized within a 40 cM region on rabbit chromosome 14 by genome scanning families of 187 rabbits in an experimental mating scheme.
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