International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases
- Author(s):
- Boycott, K.M.; Rath, A.; Chong, J.X.; Hartley, T.; Alkuraya, F.S.; Baynam, G.; Brookes, A.J.; Brudno, M.; Carracedo, A.; Dunnen, J.T. den (0000-0002-6304-1710); Dyke, S.O.M.; Estivill, X.; Goldblatt, J.; Gonthier, C.; Groft, S.C.; Gut, I.; Hamosh, A.; Hieter, P.; Hohn, S.; Hurles, M.E.; Kaufmann, P.; Knoppers, B.M.; Krischer, J.P.; Macek, M.; Matthijs, G.; Olry, A.; Parker, S.; Paschall, J.; Philippakis, A.A.; Rehm, H.L.; Robinson, P.N.; Sham, P.C.; Stefanov, R.; Taruscio, D.; Unni, D.; Vanstone, M.R.; Zhang, F.; Brunner, H.; Bamshad, M.J.; Lochmuller, H.
- Published
- 2017
- Publication type
- Article / Letter to editor
- Date issued
- 2017-05-04
- Language
- English
- Is part of
- American Journal of Human Genetics (2017), Vol. 100, no. 5, p. 695-705
- hdl
- 1887/94954
- doi
- 10.1016/j.ajhg.2017.04.003
