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: 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: McElhinney, DB Clark, BJ Weinberg, PM Kenton, ML McDonald-McGinn, D Driscoll, DA Zackai, EH Goldmuntz, E

Citation: Db. Mcelhinney et al., Association of chromosome 22q11 deletion with isolated anomalies of aorticarch laterality and branching, J AM COL C, 37(8), 2001, pp. 2114-2119

Authors: Sullivan, KE McDonald-McGinn, D Driscoll, DA Emanuel, BS Zackai, EH Jawad, AF

Citation: Ke. Sullivan et al., Longitudinal analysis of lymphocyte function and numbers in the first yearof life in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome), CL DIAG LAB, 6(6), 1999, pp. 906-911

Authors: Goldmuntz, E Clark, BJ Mitchell, LE Cuneo, BF McDonald-McGinn, D Zackair, EH Emanuel, BS Driscoll, DA

Citation: E. Goldmuntz et al., Guidelines for 22q11 deletion screening of patients with conotruncal defects - Reply, J AM COL C, 33(6), 1999, pp. 1747-1748