Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

1. Davies, R.W.
2. Fiksinski, A.M.
3. Breetvelt, E.J.
4. Williams, N.M.
5. Hooper, S.R.
6. Monfeuga, T.
7. Bassett, A.S.
8. Owen, M.J.
9. Gur, R.E.
10. Morrow, B.E.
11. McDonald-McGinn, D.M.
12. Swillen, A.
13. Chow, E.W.C.
14. van den Bree, M.
15. Emanuel, B.S.
16. Vermeesch, J.R.
17. van Amelsvoort, T.
18. Arango, C.
19. Armando, M.
20. Campbell, L.E.
21. Cubells, J.F.
22. Eliez, S.
23. Garcia-Minaur, S.
24. Gothelf, D.
25. Kates, W.R.
26. Murphy, K.C.
27. Murphy, C.M.
28. Murphy, D.G.
29. Philip, N.
30. Repetto, G.M.
31. Shashi, V.
32. Simon, T.J.
33. Suñer, D.H.
34. Vicari, S.
35. Scherer, S.W.
36. Epstein, M.P.
37. Warren, S.T.
38. Morrison, S.
39. Chawner, S.
40. Vingerhoets, C.
41. Breckpot, J.
42. Vergaelen, E.
43. Vogels, A.
44. Monks, S.
45. Prasad, S.E.
46. Sandini, C.
47. Schneider, M.
48. Maeder, J.
49. Fraguas, D.
50. Evers, R.
51. Tassone, F.
52. Morey-Canyelles, J.
53. Ousley, O.Y.
54. Antshel, K.M.
55. Fremont, W.
56. Fritsch, R.
57. Ornstein, C.
58. Daly, E.M.
59. Costain, G.A.
60. Boot, E.
61. Heung, T.
62. Crowley, T.B.
63. Zackai, E.H.
64. Calkins, M.E.
65. Gur, R.C.
66. McCabe, K.L.
67. Busa, T.
68. Schoch, K.
69. Pontillo, M.
70. Duijff, S.N.
71. Kahn, R.S.
72. Houben, M.
73. Kushan, L.
74. Jalbrzikowski, M.
75. Carmel, M.
76. Mekori-Domachevsky, E.
77. Michaelovsky, E.
78. Weinberger, R.
79. Bearden, C.E.
80. Vorstman, J.A.S.
81. Montrer des auteurs +