Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations

1. Unger, S.
2. Böhm, D.
3. Kaiser, F.J.
4. Kaulfuß, S.
5. Borozdin, W.
6. Buiting, K.
7. Burfeind, P.
8. Böhm, J.
9. Barrionuevo, F.
10. Craig, A.
11. Borowski, K.
12. Keppler-Noreuil, K.
13. Schmitt-Mechelke, T.
14. Steiner, B.
15. Bartholdi, D.
16. Lemke, J.
17. Mortier, G.
18. Sandford, R.
19. Zabel, B.
20. Superti-Furga, A.
21. Kohlhase, J.