Sentence examples for Two cnc from inspiring English sources

Exact(2)

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].

The developed parametric power models of each Therblig are tested on two CNC lathes and the results showed that the developed models can provide reliable prediction of Therblig power of CNC machine tools.

Similar(58)

An assembly based fabrication process is adopted to bond the IPMC actuators with PDMS gel using two CNC-machined molds.

Sensitivity analysis with variable variation and weight restrictions identified six CNC lathes as 'good buys' to be subsequently recommended for further consideration.

Three Cnc protein isoforms have been described, of which CncC has been suggested to play a role in redox homeostasis [24].

Overall, the CNCs work over the five domains with the least emphasis on research, however the CNCs are initiating more research and subsequent publications compared to the earlier work by O'Baugh, Wilkes, Vaughan [ 3] and three CNC's were principal investigators.

Nine CNCs are located within a 700 kbp region encompassing the OLIG1 and OLIG2 genes on chromosome 21 ENCODE region ENm005 [4] (Figure S1 and Table S1).

Fifty-two CNCs and three CMCs (Clinical Midwife Consultants) employed in an Australian metropolitan health district as of 1st January 2013 were sent an invitation.

Six CNCs (46.2%) had clerical assistance to take telephone massages, make appointments and do minimal typing and data entry.> Each of the five domains of practice was explored in the survey and the findings are depicted in tabulated form and discussed below.

Only seven CNCs (43.7%) perceived that research should be a frequent part of their role and this was confirmed by the fact that only eight (50%) did research frequently with one not doing it at all and the rest doing it occasionally Table  1.

The age at onset of thyroid cancer in two Japanese CNC patients was 72 and 73 years old, in whom PRKAR1A mutation was negative in one and not available in the other.

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