Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations
Title:
Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations
Author:
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 Dinulos, Mary Beth Flannery, David B. Fox, Michelle A. Graham Jr., John M. Grange, Dorothy K. Guttmacher, Alan E. Hannibal, Mark C. Henn, Wolfram Hennekam, RaoulC.M. Holmes, Lewis B. Hoyme, H. Eugene Leppig, Kathleen A. Lin, Angela E. MacLeod, Patrick Manchester, David K. Marcelis, Carlo Mazzanti, Laura McCann, Emma McDonald, Marie T. Mendelsohn, Nancy J. Moeschler, John B. Moghaddam, Billur Neri, Giovanni Newbury-Ecob, Ruth Pagon, Roberta A. Phillips III, John A. Sadler, Laurie S. Stoler, Joan M. Tilstra, David Walsh Vockley, Catherine M. Zackai, Elaine H. Zadeh, Touran M. Brueton, Louise Black, Graeme Charles M. Biesecker, Leslie G.