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A O Wilkie

Journal of Medical Genetics
8
Role
Title
Level Year L/R
🐜 Clinical and molecular delineation of the 17q21.31 microdeletion syndrome
50 auth. D. Koolen, Andrew J. Sharp, Andrew J. Sharp, Jane A. Hurst, H. Firth, S. Knight, A. Goldenberg, P. Saugier-Veber, R. Pfundt, L. Vissers, A. DestrΔ—e, B. Grisart, Liesbeth Rooms, N. Aa, Michael Field, ... A. Hackett, Kathleen Bell, MaΕ‚gorzata J. M. Nowaczyk, G. M. Mancini, P. Poddighe, C. Schwartz, Emilio Rossi, M. Gregori, L. Antonacci-Fulton, M. McLellan, J. Garrett, M. Wiechert, T. Miner, Seth D. Crosby, R. Ciccone, L. Willatt, Anita Rauch, Martin Zenker, S. Aradhya, Melanie A. Manning, T. Strom, J. Wagenstaller, A. Krepischi-Santos, A. Vianna-Morgante, Carla Rosenberg, S. Price, H. Stewart, C. Shaw-Smith, H. Brunner, A O Wilkie, J. Veltman, O. Zuffardi, Evan E. Eichler, Evan E. Eichler, B. Vries 		7 2008
7
🐜
🐒 Genetic screening of 202 individuals with congenital limb malformations and requiring reconstructive surgery
7 auth. D. Furniss, Shih-hsin Kan, I. B. Taylor, David W. Johnson, P. Critchley, Henk Giele, ... A O Wilkie 		5 2009
5
🐒
🐜 A cytogenetic deletion, del(17)(q11.22q21.1), in a patient with sporadic neurofibromatosis type 1 (NF1) associated with dysmorphism and developmental delay.
8 auth. M. Upadhyaya, S H Roberts, J. Maynard, E. Sorour, P. Thompson, M. Vaughan, ... A O Wilkie, H. E. Hughes 		5 1996
5
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