International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases

  1. Boycott, K.M.
  2. Rath, A.
  3. Chong, J.X.
  4. Hartley, T.
  5. Alkuraya, F.S.
  6. Baynam, G.
  7. Brookes, A.J.
  8. Brudno, M.
  9. Carracedo, A.
  10. den Dunnen, J.T.
  11. Dyke, S.O.M.
  12. Estivill, X.
  13. Goldblatt, J.
  14. Gonthier, C.
  15. Groft, S.C.
  16. Gut, I.
  17. Hamosh, A.
  18. Hieter, P.
  19. Höhn, S.
  20. Hurles, M.E.
  21. Kaufmann, P.
  22. Knoppers, B.M.
  23. Krischer, J.P.
  24. Macek, M.
  25. Matthijs, G.
  26. Olry, A.
  27. Parker, S.
  28. Paschall, J.
  29. Philippakis, A.A.
  30. Rehm, H.L.
  31. Robinson, P.N.
  32. Sham, P.-C.
  33. Stefanov, R.
  34. Taruscio, D.
  35. Unni, D.
  36. Vanstone, M.R.
  37. Zhang, F.
  38. Brunner, H.
  39. Bamshad, M.J.
  40. Lochmüller, H.
  41. Show all authors +
Journal:
American Journal of Human Genetics

ISSN: 1537-6605 0002-9297

Year of publication: 2017

Volume: 100

Issue: 5

Pages: 695-705

Type: Note

DOI: 10.1016/J.AJHG.2017.04.003 GOOGLE SCHOLAR lock_openOpen access editor

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