Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

Background: The chromosome 17q21.31 microdeletion syndrome is a novel genomic disorder that has originally been identified using high resolution genome analyses in patients with unexplained mental retardation. Aim: We report the molecular and/or clinical characterisation of 22 individuals with the 1...

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المؤلفون الرئيسيون:	Koolen, D, Sharp, A, Hurst, J, Firth, H, Knight, S, Goldenberg, A, Saugier-Veber, P, Pfundt, R, Vissers, L, Destree, A, Grisart, B, Rooms, L, Van der Aa, N, Field, M, Hackett, A, Bell, K, Nowaczyk, M, Mancini, G, Poddighe, P, Schwartz, C, Rossi, E, De Gregori, M, Antonacci-Fulton, L, Ii, M, Garrett, J
التنسيق:	Journal article
اللغة:	English
منشور في:	2008

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

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