1 | distribution | 9,017 |
2 | distributions | 1,399 |
3 | integrals | 124 |
4 | minima | 64 |
5 | inhomogeneity | 60 |
6 | autocorrelation | 56 |
7 | evolvement | 19 |
8 | secretome | 15 |
9 | engagements | 9 |
10 | apioside | 8 |
11 | toxigenicity | 8 |
12 | colouration | 7 |
13 | fracture-dislocation | 6 |
14 | 40/.04 | 5 |
15 | dependance | 5 |
16 | affix | 3 |
17 | pitt-2000 | 3 |
18 | technigue | 3 |
19 | *group | 2 |
20 | 58years | 2 |
21 | beta-globulin | 2 |
22 | bikini | 2 |
23 | chelicerae | 2 |
24 | electromagnetism | 2 |
25 | myomeric | 2 |
26 | resolvability | 2 |
27 | s.p.a | 2 |
28 | shrinker | 2 |
29 | sibthorpioides | 2 |
30 | ұ | 2 |
31 | 2,5-dkcmo- | 1 |
32 | 45-48°c | 1 |
33 | 47.5±14.1 | 1 |
34 | 49.5years | 1 |
35 | 52.8±2.89 | 1 |
36 | 55.85±10.74 | 1 |
37 | birchmanni | 1 |
38 | c6f5- | 1 |
39 | conducing | 1 |
40 | effectiveness-risk | 1 |
41 | features-prosodic/suprasegmental-but | 1 |
42 | fruit-color | 1 |
43 | increae | 1 |
44 | inversions-layers | 1 |
45 | length/phase | 1 |
46 | log-kill | 1 |
47 | nfat/ap-1- | 1 |
48 | promylagaulinae | 1 |
49 | repair.journal | 1 |
50 | self-categorizations | 1 |
51 | stopage | 1 |
52 | traditionalism | 1 |
1 | *group | 2 |
2 | 2,5-dkcmo- | 1 |
3 | 40/.04 | 5 |
4 | 45-48°c | 1 |
5 | 47.5±14.1 | 1 |
6 | 49.5years | 1 |
7 | 52.8±2.89 | 1 |
8 | 55.85±10.74 | 1 |
9 | 58years | 2 |
10 | affix | 3 |
11 | apioside | 8 |
12 | autocorrelation | 56 |
13 | beta-globulin | 2 |
14 | bikini | 2 |
15 | birchmanni | 1 |
16 | c6f5- | 1 |
17 | chelicerae | 2 |
18 | colouration | 7 |
19 | conducing | 1 |
20 | dependance | 5 |
21 | distribution | 9,017 |
22 | distributions | 1,399 |
23 | effectiveness-risk | 1 |
24 | electromagnetism | 2 |
25 | engagements | 9 |
26 | evolvement | 19 |
27 | features-prosodic/suprasegmental-but | 1 |
28 | fracture-dislocation | 6 |
29 | fruit-color | 1 |
30 | increae | 1 |
31 | inhomogeneity | 60 |
32 | integrals | 124 |
33 | inversions-layers | 1 |
34 | length/phase | 1 |
35 | log-kill | 1 |
36 | minima | 64 |
37 | myomeric | 2 |
38 | nfat/ap-1- | 1 |
39 | pitt-2000 | 3 |
40 | promylagaulinae | 1 |
41 | repair.journal | 1 |
42 | resolvability | 2 |
43 | s.p.a | 2 |
44 | secretome | 15 |
45 | self-categorizations | 1 |
46 | shrinker | 2 |
47 | sibthorpioides | 2 |
48 | stopage | 1 |
49 | technigue | 3 |
50 | toxigenicity | 8 |
51 | traditionalism | 1 |
52 | ұ | 2 |
1 | nfat/ap-1- | 1 |
2 | c6f5- | 1 |
3 | 2,5-dkcmo- | 1 |
4 | pitt-2000 | 3 |
5 | 47.5±14.1 | 1 |
6 | 40/.04 | 5 |
7 | 55.85±10.74 | 1 |
8 | 52.8±2.89 | 1 |
9 | s.p.a | 2 |
10 | minima | 64 |
11 | myomeric | 2 |
12 | 45-48°c | 1 |
13 | increae | 1 |
14 | promylagaulinae | 1 |
15 | chelicerae | 2 |
16 | dependance | 5 |
17 | apioside | 8 |
18 | stopage | 1 |
19 | secretome | 15 |
20 | length/phase | 1 |
21 | technigue | 3 |
22 | conducing | 1 |
23 | bikini | 2 |
24 | birchmanni | 1 |
25 | effectiveness-risk | 1 |
26 | repair.journal | 1 |
27 | log-kill | 1 |
28 | traditionalism | 1 |
29 | electromagnetism | 2 |
30 | beta-globulin | 2 |
31 | fracture-dislocation | 6 |
32 | autocorrelation | 56 |
33 | colouration | 7 |
34 | distribution | 9,017 |
35 | *group | 2 |
36 | shrinker | 2 |
37 | fruit-color | 1 |
38 | sibthorpioides | 2 |
39 | integrals | 124 |
40 | self-categorizations | 1 |
41 | distributions | 1,399 |
42 | 49.5years | 1 |
43 | 58years | 2 |
44 | inversions-layers | 1 |
45 | engagements | 9 |
46 | evolvement | 19 |
47 | features-prosodic/suprasegmental-but | 1 |
48 | affix | 3 |
49 | toxigenicity | 8 |
50 | inhomogeneity | 60 |
51 | resolvability | 2 |
52 | ұ | 2 |