1. Clinical and molecular delineation of the 17q21.31 microdeletion syndrome
- Author
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Koolen, D.A., Sharp, A.J., Hurst, J.A., Firth, H.V., Knight, S.J.L., Goldenberg, A., Saugier-Veber, P., Pfundt, R., Vissers, L.E.L.M., Destree, A., Grisart, B., Rooms, L., Van der Aa, N., Field, M., Hackett, A., Bell, K., Nowaczyk, M.J.M., Mancini, G.M.S., Poddighe, P.J., Schwartz, C.E., Rossi, E., De Gregori, M., Antonacci-Fulton, L.L., McLellan, M.D., II, Garrett, J.M., Wiechert, M.A., Miner, T.L., Crosby, S., Ciccone, R., Willatt, L., Rauch, A., Zenker, M., Aradhya, S., Manning, M.A., Strom, T.M., Wagenstaller, J., Krepischi-Santos, A.C., Vianna-Morgante, A.M., Rosenberg, C., Price, S.M., Stewart, H., Shaw-Smith, C., H.G. Brunner, Wilkie, A.O.M., Veltman, J.A., Zuffardi, O., Eichler, E.E., and de Vries, B.B.A.
- Subjects
Chromosomes -- Research ,Chromosomes -- Physiological aspects ,Genetic disorders -- Research ,Genetic disorders -- Physiological aspects ,Mental retardation -- Research ,Mental retardation -- Genetic aspects ,Health - Published
- 2008