Authors: Johnston, Jennifer J. Olivos-Glander, Isabelle Killoran, Christina Elson, Emma Turner, Joyce T. Peters, Kathryn F. Abbott, Margaret H. Aughton, David J. Aylsworth, Arthur S. Bamshad, Michael J. Booth, Carol Curry, Cynthia J. David, Albert Binulos, Mary Beth Flannery, David B. Fox, Michelle A. Graham, John M. Jr. Grange, Dorothy K. Guttmacher, Alan E. Hannibal, Mark C. Henn, Wolfram Hennekam, Raoul C.M. Holmes, Lewis B. Eugene Hoyme, H. Leppig, Kathleen A. Lin, Angela E. MacLeod, Patrick Manchester, David K. Marcelis, Carlo Mazzanti, Laura McCann, Laura McDonald, Marie T. Mendelsohn, Nancy J. Moeschler, John B. Moghaddam, Billur Neri, Giovanni Newbury-Ecob, Ruth Pagon, Roberta A. Philips, John A. III Sadler, Laurie S. Stoler, Joan M. Tilstra, David Walsh Vockley, Catherine M. Zachai, Elaine H. Zadeh, Touran M. Brueton, Louise Black, Graeme Charles M. Biesecker, Leslie G.

Citation: J. Johnston, Jennifer et al., Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations, American journal of human genetics , 76(4), 2005, pp. 609-622

Authors: Ensenauer, Regina E. Adeyinka, Adewale Flynn, Heather C. Michels, Virginia V. Lindor, Noralene M. Dawson, D. Brian Thorland, Erik C. Smith, Wendy E. Simon- Fayard, ELba Alexander, Alan A. Kulharya, Anita S. Ketterling, Rhett P. Clark, Robin D. Jalal, Syed M. Pham Lorentz, Cindy Goldstein, Jennifer L. McDonald, Marie T.

Citation: E. Ensenauer, Regina et al., Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients, American journal of human genetics , 73(5), 2003, pp. 1027-1040