1995-96 Regular Season
Rk | G | Date | Age | Tm | Opp | GS | MP | TS% | eFG% | ORB% | DRB% | TRB% | AST% | STL% | BLK% | TOV% | USG% | ORtg | DRtg | GmSc | BPM | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | 1 | 1995-11-03 | 25-056 | PHI | WSB | W (+2) | 1 | 42:00 | .610 | .545 | 21.9 | 14.9 | 18.4 | 7.3 | 5.8 | 0.0 | 25.0 | 23.2 | 108 | 98 | 21.2 | 1.0 | |
2 | 2 | 1995-11-04 | 25-057 | PHI | @ | CHH | L (-11) | 1 | 42:00 | .653 | .643 | 9.5 | 17.0 | 13.8 | 3.7 | 3.2 | 1.5 | 11.5 | 16.4 | 125 | 106 | 18.8 | 3.7 |
3 | 3 | 1995-11-17 | 25-070 | PHI | CLE | L (-32) | 1 | 21:00 | 1.025 | 1.000 | 0.0 | 5.9 | 3.0 | 9.4 | 0.0 | 0.0 | 45.0 | 9.7 | 104 | 131 | 3.0 | -4.6 | |
4 | 4 | 1995-11-18 | 25-071 | PHI | @ | NJN | L (-16) | 1 | 41:00 | .612 | .615 | 5.6 | 15.4 | 11.4 | 10.8 | 0.0 | 0.0 | 6.7 | 16.9 | 128 | 110 | 13.7 | 0.7 |
5 | 5 | 1995-11-22 | 25-075 | PHI | HOU | L (-9) | 1 | 40:00 | .577 | .563 | 9.6 | 32.7 | 18.8 | 7.9 | 0.0 | 0.0 | 5.2 | 19.5 | 132 | 126 | 17.3 | 0.0 | |
6 | 6 | 1995-11-24 | 25-077 | PHI | @ | DET | L (-23) | 1 | 25:00 | .392 | .273 | 4.2 | 12.4 | 7.5 | 8.3 | 2.0 | 0.0 | 0.0 | 22.2 | 92 | 107 | 6.1 | -1.5 |
7 | 7 | 1995-11-25 | 25-078 | PHI | GSW | L (-18) | 1 | 32:00 | .560 | .462 | 15.6 | 11.8 | 14.0 | 12.0 | 0.0 | 0.0 | 5.9 | 23.1 | 123 | 120 | 14.9 | 1.5 | |
8 | 8 | 1995-11-29 | 25-082 | PHI | @ | ATL | L (-25) | 1 | 33:00 | .437 | .429 | 9.1 | 26.4 | 16.2 | 7.2 | 6.3 | 0.0 | 11.8 | 21.9 | 92 | 103 | 11.4 | 1.8 |
9 | 9 | 1995-12-01 | 25-084 | PHI | @ | TOR | L (-3) | 1 | 41:00 | .280 | .222 | 0.0 | 13.8 | 5.7 | 8.5 | 5.0 | 0.0 | 0.0 | 14.0 | 68 | 110 | 5.7 | -7.8 |
10 | 10 | 1995-12-02 | 25-085 | PHI | NYK | L (-9) | 1 | 41:00 | .433 | .400 | 14.9 | 22.3 | 18.4 | 9.9 | 2.5 | 1.6 | 4.2 | 25.9 | 101 | 98 | 16.5 | 3.0 | |
11 | 11 | 1995-12-05 | 25-088 | PHI | @ | IND | L (-17) | 1 | 43:00 | .376 | .375 | 10.1 | 15.5 | 12.9 | 17.4 | 2.6 | 0.0 | 22.0 | 15.2 | 83 | 121 | 6.2 | -4.0 |
12 | 12 | 1995-12-06 | 25-089 | PHI | DAL | W (+21) | 0 | 34:00 | .400 | .286 | 11.8 | 22.3 | 17.5 | 14.8 | 1.5 | 4.3 | 18.6 | 13.8 | 100 | 86 | 10.8 | -3.1 | |
13 | 13 | 1995-12-08 | 25-091 | PHI | @ | CLE | L (-28) | 0 | 29:00 | .875 | .875 | 5.3 | 34.8 | 21.6 | 16.2 | 0.0 | 5.8 | 27.3 | 18.4 | 116 | 117 | 12.9 | 4.8 |
14 | 14 | 1995-12-09 | 25-092 | PHI | BOS | L (-26) | 1 | 43:00 | .396 | .250 | 6.3 | 17.6 | 11.0 | 3.8 | 0.0 | 0.0 | 10.9 | 16.2 | 86 | 116 | 5.6 | -8.3 | |
15 | 15 | 1995-12-11 | 25-094 | PHI | DEN | L (-13) | 1 | 45:00 | .682 | .636 | 4.2 | 18.2 | 10.4 | 4.5 | 1.2 | 1.7 | 13.2 | 15.6 | 124 | 117 | 15.0 | 0.2 | |
16 | 16 | 1995-12-13 | 25-096 | PHI | @ | BOS | L (-11) | 1 | 30:00 | .603 | .571 | 0.0 | 7.8 | 4.2 | 0.0 | 0.0 | 0.0 | 20.2 | 29.9 | 92 | 121 | 6.2 | -9.6 |
17 | 17 | 1995-12-17 | 25-100 | PHI | @ | MIN | W (+2) | 1 | 48:00 | .637 | .583 | 8.3 | 17.8 | 13.6 | 25.9 | 2.2 | 3.8 | 22.4 | 22.4 | 118 | 104 | 21.3 | 3.5 |
18 | 18 | 1995-12-20 | 25-103 | PHI | UTA | W (+4) | 1 | 43:00 | .638 | .600 | 5.9 | 14.9 | 9.8 | 4.6 | 0.0 | 5.3 | 20.3 | 15.6 | 110 | 112 | 10.8 | -0.9 | |
19 | 19 | 1995-12-22 | 25-105 | PHI | MIL | L (-5) | 1 | 46:00 | .512 | .412 | 5.2 | 32.6 | 17.4 | 7.5 | 2.3 | 0.0 | 16.3 | 25.6 | 93 | 107 | 14.5 | -4.8 | |
20 | 20 | 1995-12-23 | 25-106 | PHI | NJN | L (-13) | 1 | 35:00 | .313 | .182 | 6.4 | 32.3 | 17.8 | 19.4 | 0.0 | 0.0 | 7.3 | 19.5 | 81 | 107 | 5.1 | -6.8 | |
Rk | G | Date | Age | Tm | Opp | GS | MP | TS% | eFG% | ORB% | DRB% | TRB% | AST% | STL% | BLK% | TOV% | USG% | ORtg | DRtg | GmSc | BPM | ||
21 | 21 | 1995-12-27 | 25-110 | PHI | @ | PHO | L (-15) | 1 | 45:00 | .714 | .667 | 5.9 | 14.2 | 10.5 | 4.5 | 1.3 | 1.5 | 26.3 | 17.3 | 107 | 125 | 12.5 | -4.6 |
22 | 22 | 1995-12-29 | 25-112 | PHI | @ | SAC | L (-20) | 1 | 37:00 | .823 | .818 | 10.2 | 10.0 | 10.1 | 12.2 | 1.4 | 4.3 | 13.6 | 18.0 | 147 | 123 | 21.3 | 6.5 |
23 | 23 | 1995-12-30 | 25-113 | PHI | @ | DEN | L (-8) | 1 | 41:00 | .480 | .385 | 9.2 | 13.4 | 11.2 | 0.0 | 0.0 | 0.0 | 6.0 | 18.0 | 109 | 125 | 8.2 | -7.8 |
24 | 24 | 1996-01-02 | 25-116 | PHI | @ | LAL | W (+1) | 1 | 47:00 | .395 | .308 | 5.1 | 23.4 | 15.1 | 13.2 | 0.0 | 5.4 | 20.8 | 18.8 | 81 | 97 | 9.6 | -3.0 |
25 | 25 | 1996-01-03 | 25-117 | PHI | @ | GSW | L (-11) | 1 | 43:00 | .367 | .182 | 9.3 | 19.5 | 14.7 | 5.5 | 1.1 | 1.5 | 18.0 | 15.8 | 84 | 118 | 5.8 | -7.8 |
26 | 26 | 1996-01-05 | 25-119 | PHI | @ | VAN | L (-1) | 1 | 47:00 | .597 | .533 | 10.7 | 32.2 | 23.0 | 12.1 | 1.1 | 4.2 | 23.0 | 20.6 | 104 | 90 | 18.9 | 2.4 |
27 | 27 | 1996-01-10 | 25-124 | PHI | WSB | L (-5) | 1 | 47:00 | .394 | .375 | 7.7 | 29.9 | 20.8 | 0.0 | 0.0 | 1.4 | 10.1 | 18.1 | 82 | 91 | 9.1 | -5.9 | |
28 | 28 | 1996-01-12 | 25-126 | PHI | @ | NJN | W (+27) | 1 | 26:00 | .854 | .833 | 0.0 | 30.2 | 17.7 | 11.3 | 2.0 | 0.0 | 23.7 | 14.2 | 128 | 76 | 9.9 | 4.8 |
29 | 29 | 1996-01-13 | 25-127 | PHI | CHI | L (-27) | 1 | 37:00 | .678 | .615 | 10.2 | 8.3 | 9.2 | 5.1 | 4.1 | 0.0 | 21.3 | 22.9 | 110 | 124 | 16.0 | 0.8 | |
30 | 30 | 1996-01-16 | 25-130 | PHI | @ | CHI | L (-12) | 1 | 37:00 | .415 | .429 | 6.3 | 9.1 | 7.7 | 3.6 | 0.0 | 0.0 | 0.0 | 11.5 | 103 | 131 | 4.9 | -6.8 |
31 | 31 | 1996-01-17 | 25-131 | PHI | MIL | L (-11) | 1 | 48:00 | .750 | .750 | 0.0 | 18.2 | 9.5 | 8.3 | 4.4 | 0.0 | 42.9 | 13.8 | 84 | 118 | 8.7 | -3.4 | |
32 | 32 | 1996-01-19 | 25-133 | PHI | ATL | L (-5) | 1 | 41:00 | .253 | .273 | 18.2 | 18.6 | 18.4 | 8.8 | 1.4 | 0.0 | 7.8 | 14.4 | 79 | 95 | 5.9 | -4.4 | |
33 | 33 | 1996-01-21 | 25-135 | PHI | SAS | L (-30) | 1 | 43:00 | .594 | .538 | 8.6 | 31.0 | 16.6 | 18.5 | 1.2 | 4.9 | 12.3 | 15.4 | 124 | 122 | 19.9 | 2.5 | |
34 | 34 | 1996-01-23 | 25-137 | PHI | @ | ORL | L (-15) | 1 | 36:00 | .441 | .167 | 13.3 | 14.4 | 13.8 | 9.8 | 1.5 | 2.5 | 14.2 | 25.1 | 103 | 120 | 12.0 | -2.9 |
35 | 35 | 1996-01-24 | 25-138 | PHI | CLE | L (-3) | 1 | 47:00 | .679 | .571 | 11.7 | 16.0 | 13.7 | 17.9 | 1.3 | 2.0 | 9.8 | 23.3 | 139 | 114 | 23.6 | 7.8 | |
36 | 36 | 1996-01-26 | 25-140 | PHI | LAL | L (-12) | 1 | 44:00 | .648 | .625 | 0.0 | 24.5 | 12.4 | 18.1 | 3.7 | 0.0 | 14.5 | 23.9 | 109 | 104 | 19.7 | 3.4 | |
37 | 37 | 1996-01-27 | 25-141 | PHI | @ | CHH | L (-5) | 1 | 47:00 | .660 | .545 | 4.5 | 26.1 | 15.1 | 10.3 | 1.1 | 4.8 | 6.8 | 14.2 | 140 | 114 | 19.6 | 2.5 |
38 | 38 | 1996-01-29 | 25-143 | PHI | VAN | W (+11) | 1 | 47:00 | .573 | .529 | 5.8 | 19.9 | 13.4 | 3.5 | 2.3 | 6.3 | 9.1 | 21.8 | 115 | 100 | 20.4 | -2.4 | |
39 | 39 | 1996-02-01 | 25-146 | PHI | @ | MIA | L (-20) | 1 | 45:00 | .564 | .438 | 5.2 | 26.7 | 15.2 | 9.5 | 1.2 | 0.0 | 8.6 | 23.6 | 117 | 130 | 16.9 | -3.5 |
40 | 40 | 1996-02-03 | 25-148 | PHI | POR | L (-11) | 1 | 42:00 | .500 | .500 | 11.9 | 10.6 | 11.3 | 0.0 | 3.7 | 5.0 | 10.0 | 21.2 | 98 | 96 | 15.2 | 2.3 | |
Rk | G | Date | Age | Tm | Opp | GS | MP | TS% | eFG% | ORB% | DRB% | TRB% | AST% | STL% | BLK% | TOV% | USG% | ORtg | DRtg | GmSc | BPM | ||
41 | 41 | 1996-02-07 | 25-152 | PHI | IND | W (+1) | 1 | 44:00 | .678 | .692 | 15.2 | 7.0 | 10.5 | 12.5 | 1.3 | 4.6 | 11.9 | 18.6 | 133 | 122 | 20.5 | 3.6 | |
42 | 42 | 1996-02-13 | 25-158 | PHI | @ | MIL | W (+3) | 1 | 41:00 | .625 | .400 | 7.6 | 13.0 | 10.5 | 4.4 | 1.2 | 4.6 | 17.2 | 18.6 | 119 | 101 | 15.3 | -0.4 |
43 | 43 | 1996-02-14 | 25-159 | PHI | DET | L (-19) | 1 | 46:00 | .249 | .154 | 7.6 | 21.5 | 12.9 | 23.3 | 2.3 | 5.7 | 15.7 | 18.8 | 68 | 108 | 7.9 | -3.7 | |
44 | 44 | 1996-02-16 | 25-161 | PHI | @ | NYK | L (-32) | 1 | 31:00 | .630 | .600 | 0.0 | 13.3 | 5.7 | 8.6 | 3.2 | 0.0 | 0.0 | 23.7 | 120 | 121 | 16.3 | 5.1 |
45 | 45 | 1996-02-17 | 25-162 | PHI | @ | CLE | L (-15) | 1 | 37:00 | .571 | .571 | 6.8 | 19.7 | 12.8 | 31.4 | 1.7 | 8.5 | 20.2 | 14.3 | 119 | 119 | 12.3 | 4.4 |
46 | 46 | 1996-02-20 | 25-165 | PHI | @ | ORL | L (-19) | 0 | 31:00 | .636 | .636 | 12.6 | 22.1 | 16.6 | 5.3 | 1.6 | 0.0 | 0.0 | 14.9 | 146 | 125 | 14.7 | 3.7 |
47 | 47 | 1996-02-21 | 25-166 | PHI | MIA | L (-9) | 1 | 34:00 | .400 | .400 | 11.1 | 35.3 | 22.3 | 0.0 | 1.7 | 2.2 | 0.0 | 7.3 | 102 | 71 | 8.3 | 1.0 | |
48 | 48 | 1996-02-23 | 25-168 | PHI | @ | IND | L (-7) | 1 | 45:00 | .506 | .500 | 11.2 | 20.2 | 15.6 | 4.0 | 2.5 | 1.5 | 15.5 | 13.6 | 103 | 112 | 10.3 | -2.8 |
49 | 49 | 1996-02-25 | 25-170 | PHI | @ | MIA | L (-7) | 1 | 42:00 | .552 | .467 | 15.0 | 8.4 | 11.6 | 10.7 | 3.7 | 3.9 | 5.5 | 18.9 | 133 | 118 | 20.8 | 3.9 |
50 | 50 | 1996-02-27 | 25-172 | PHI | @ | DAL | W (+6) | 1 | 42:00 | .527 | .522 | 5.0 | 22.0 | 14.0 | 11.7 | 3.3 | 3.9 | 13.5 | 28.8 | 103 | 103 | 20.6 | -0.1 |
51 | 51 | 1996-02-29 | 25-174 | PHI | @ | HOU | L (-14) | 1 | 40:00 | .579 | .400 | 12.5 | 14.3 | 13.3 | 8.6 | 0.0 | 12.0 | 12.6 | 25.1 | 121 | 117 | 22.3 | 6.1 |
52 | 52 | 1996-03-02 | 25-176 | PHI | @ | SAS | L (-14) | 1 | 40:00 | .758 | .727 | 3.3 | 17.1 | 10.8 | 8.8 | 1.2 | 3.8 | 12.1 | 17.8 | 138 | 115 | 19.4 | 4.7 |
53 | 53 | 1996-03-04 | 25-178 | PHI | ORL | L (-13) | 1 | 29:00 | .514 | .400 | 7.0 | 14.7 | 10.8 | 30.2 | 0.0 | 2.5 | 13.7 | 21.5 | 116 | 121 | 11.2 | 2.5 | |
54 | 54 | 1996-03-06 | 25-180 | PHI | MIN | L (-13) | 1 | 38:00 | .275 | .238 | 4.8 | 24.2 | 13.9 | 0.0 | 0.0 | 3.4 | 4.1 | 27.0 | 66 | 108 | 2.8 | -11.1 | |
55 | 55 | 1996-03-08 | 25-182 | PHI | NYK | W (+8) | 1 | 45:00 | .396 | .300 | 5.9 | 28.1 | 17.3 | 0.0 | 3.6 | 3.2 | 24.0 | 17.6 | 72 | 98 | 7.0 | -8.7 | |
56 | 56 | 1996-03-10 | 25-184 | PHI | LAC | L (-2) | 1 | 39:00 | .556 | .474 | 11.4 | 27.7 | 19.3 | 5.4 | 4.0 | 1.9 | 4.1 | 28.1 | 121 | 105 | 22.8 | 3.9 | |
57 | 57 | 1996-03-12 | 25-186 | PHI | TOR | W (+8) | 1 | 40:00 | .362 | .333 | 13.0 | 24.7 | 18.0 | 0.0 | 0.0 | 2.0 | 24.3 | 16.4 | 77 | 117 | 3.7 | -13.1 | |
58 | 58 | 1996-03-13 | 25-187 | PHI | @ | BOS | L (-10) | 1 | 40:00 | .526 | .462 | 7.7 | 16.0 | 11.7 | 17.3 | 0.0 | 1.9 | 0.0 | 15.7 | 133 | 116 | 13.9 | 1.0 |
59 | 59 | 1996-03-15 | 25-189 | PHI | PHO | L (-26) | 1 | 36:00 | .375 | .333 | 5.0 | 22.2 | 11.2 | 15.8 | 5.4 | 3.7 | 18.4 | 18.5 | 81 | 119 | 9.3 | -3.2 | |
60 | 60 | 1996-03-16 | 25-190 | PHI | @ | NYK | L (-6) | 1 | 40:00 | .593 | .500 | 9.6 | 30.6 | 23.7 | 9.2 | 0.0 | 0.0 | 13.7 | 18.9 | 118 | 104 | 13.5 | 1.3 |
Rk | G | Date | Age | Tm | Opp | GS | MP | TS% | eFG% | ORB% | DRB% | TRB% | AST% | STL% | BLK% | TOV% | USG% | ORtg | DRtg | GmSc | BPM | ||
61 | 61 | 1996-03-18 | 25-192 | PHI | CHI | L (-4) | 1 | 38:00 | .448 | .308 | 16.1 | 21.6 | 18.7 | 0.0 | 2.9 | 1.9 | 6.0 | 20.4 | 109 | 106 | 14.5 | 1.3 | |
62 | 62 | 1996-03-20 | 25-194 | PHI | @ | UTA | L (-23) | 1 | 34:00 | .549 | .455 | 6.0 | 12.5 | 8.7 | 37.3 | 0.0 | 2.0 | 13.6 | 19.1 | 118 | 120 | 12.4 | 4.4 |
63 | 63 | 1996-03-22 | 25-196 | PHI | @ | LAC | L (-14) | 1 | 40:00 | .570 | .429 | 16.0 | 18.9 | 17.3 | 0.0 | 2.6 | 7.2 | 16.0 | 26.4 | 113 | 109 | 21.0 | 4.5 |
64 | 64 | 1996-03-23 | 25-197 | PHI | @ | SEA | L (-40) | 1 | 42:00 | .445 | .438 | 15.9 | 11.4 | 14.1 | 9.1 | 2.4 | 0.0 | 9.5 | 21.6 | 97 | 137 | 12.7 | -3.8 |
65 | 65 | 1996-03-25 | 25-199 | PHI | @ | POR | L (-23) | 1 | 35:00 | .458 | .412 | 17.1 | 22.3 | 19.6 | 8.4 | 4.7 | 2.2 | 4.4 | 30.2 | 104 | 97 | 18.2 | 9.2 |
66 | 66 | 1996-03-27 | 25-201 | PHI | TOR | W (+9) | 1 | 39:00 | .676 | .600 | 0.0 | 16.6 | 9.8 | 4.4 | 1.4 | 3.8 | 12.6 | 30.3 | 118 | 104 | 21.5 | -1.0 | |
67 | 67 | 1996-03-29 | 25-203 | PHI | BOS | L (-6) | 1 | 27:00 | .776 | .750 | 11.9 | 11.9 | 11.9 | 0.0 | 2.0 | 8.3 | 28.0 | 29.3 | 105 | 109 | 14.7 | 1.3 | |
68 | 68 | 1996-03-30 | 25-204 | PHI | @ | WSB | L (-2) | 1 | 41:00 | .751 | .714 | 12.3 | 13.0 | 12.7 | 0.0 | 1.3 | 3.6 | 6.1 | 18.4 | 150 | 121 | 21.4 | 3.6 |
69 | 69 | 1996-04-03 | 25-208 | PHI | IND | L (-15) | 1 | 43:00 | .539 | .467 | 3.2 | 24.5 | 14.7 | 4.3 | 4.0 | 1.4 | 0.0 | 21.0 | 115 | 107 | 18.3 | 3.0 | |
70 | 70 | 1996-04-05 | 25-210 | PHI | DET | L (-21) | 1 | 40:00 | .667 | .667 | 10.7 | 29.1 | 18.5 | 0.0 | 1.4 | 6.9 | 21.1 | 22.0 | 103 | 120 | 16.2 | 0.0 | |
71 | 71 | 1996-04-06 | 25-211 | PHI | @ | ATL | W (+1) | 1 | 46:00 | .640 | .500 | 12.6 | 24.6 | 18.7 | 10.5 | 0.0 | 0.0 | 5.7 | 18.1 | 144 | 116 | 19.7 | 2.9 |
72 | 72 | 1996-04-08 | 25-213 | PHI | NJN | W (+3) | 1 | 44:00 | .288 | .308 | 8.9 | 13.0 | 10.8 | 22.1 | 5.1 | 3.1 | 33.5 | 22.4 | 57 | 85 | 4.7 | -6.7 | |
73 | 73 | 1996-04-10 | 25-215 | PHI | @ | DET | L (-16) | 1 | 44:00 | .543 | .526 | 12.1 | 11.2 | 11.7 | 0.0 | 2.6 | 1.9 | 8.3 | 28.4 | 106 | 110 | 18.5 | 3.1 |
74 | 74 | 1996-04-12 | 25-217 | PHI | @ | CHI | L (-30) | 1 | 39:00 | .504 | .500 | 6.8 | 22.4 | 14.3 | 15.8 | 1.5 | 2.1 | 21.2 | 24.2 | 91 | 131 | 9.8 | -2.5 |
75 | 75 | 1996-04-14 | 25-219 | PHI | CHH | L (-16) | 1 | 40:00 | .506 | .444 | 2.9 | 30.0 | 16.3 | 5.4 | 2.9 | 0.0 | 0.0 | 25.2 | 108 | 107 | 16.6 | 3.5 | |
76 | 76 | 1996-04-17 | 25-222 | PHI | MIA | W (+4) | 1 | 43:00 | .704 | .688 | 6.4 | 18.6 | 12.6 | 14.1 | 5.1 | 3.8 | 18.4 | 24.9 | 114 | 92 | 23.3 | 7.8 | |
77 | 77 | 1996-04-19 | 25-224 | PHI | ORL | L (-20) | 1 | 34:00 | .503 | .471 | 3.1 | 35.3 | 16.3 | 14.3 | 1.6 | 2.2 | 5.3 | 25.8 | 105 | 121 | 13.3 | -0.8 | |
78 | 78 | 1996-04-21 | 25-226 | PHI | @ | TOR | W (+4) | 1 | 46:00 | .576 | .538 | 14.7 | 19.6 | 17.2 | 12.4 | 1.1 | 11.4 | 6.2 | 30.4 | 127 | 102 | 32.2 | 7.6 |
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