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Results: 1-6 |
Results: 6

Authors: Bearden, CE Woodin, MF Wang, PP Moss, E McDonald-McGinn, D Zackai, E Emannuel, B Cannon, TD
Citation: Ce. Bearden et al., The neurocognitive phenotype of the 22Q11.2 deletion syndrome: Selective deficit in visual-spatial memory, J CL EXP N, 23(4), 2001, pp. 447-464

Authors: Barlow, GM Chen, XN Shi, ZY Lyons, GE Kurnit, DM Celle, L Spinner, NB Zackai, E Pettenati, MJ Van Riper, AJ Vekemans, MJ Mjaatvedt, CH Korenberg, JR
Citation: Gm. Barlow et al., Down syndrome congenital heart disease: A narrowed region and a candidate gene, GENET MED, 3(2), 2001, pp. 91-101

Authors: Woodin, M Wang, PP Aleman, D McDonald-McGinn, D Zackai, E Moss, E
Citation: M. Woodin et al., Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion, GENET MED, 3(1), 2001, pp. 34-39

Authors: Markowitz, RI Zackai, E
Citation: Ri. Markowitz et E. Zackai, A pragmatic approach to the radiologic diagnosis of pediatric syndromes and skeletal dysplasias, RAD CLIN NA, 39(4), 2001, pp. 791

Authors: Jawad, AF McDonald-McGinn, DM Zackai, E Sullivan, KE
Citation: Af. Jawad et al., Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome), J PEDIAT, 139(5), 2001, pp. 715-723

Authors: Faivre, L Le Merrer, M Baumann, C Polak, M Chatelain, P Sulmont, V Cousin, J Bost, M Cordier, MP Zackai, E Russell, K Finidori, G Pouliquen, JC Munnich, A Maroteaux, P Cormier-Daire, V
Citation: L. Faivre et al., Acromicric dysplasia: long term outcome and evidence of autosomal dominantinheritance, J MED GENET, 38(11), 2001, pp. 745-749
Risultati: 1-6 |