Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.
Koolen, D. A.; Sharp, A. J.; Hurst, J. A.; Firth, H. V.; Knight, S. J. L.; Goldenberg, A.; Saugier-Veber, P.; Pfundt, A.; Vissers, L. E. L. M.; Destrée, 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.; Journal of Medical Genetics, 2008, vol. 45, issue 11, p 710, ISSN 00222593. ISBN 14686244.

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