Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GL13 mutations

JJ Johnston, I Olivos-Glander, C Killoran, E Elson, JT Turner, KF Peters, MH Abbott, DJ Aughton, AS Avisworth, MJ Bamshad, C Booth, CJ Curry, A David, MB Dinulos, DB Flannery, MA Fox, JM Graham, DK Grange, AE Guttmacher, MC HannibalW Henn, RC Hennekam, LB Holmes, HE Hovme, KA Leppia, AE Lin, P Macleod, DK Manchester, C Marcelis, L Mazzanti, E McCann, MT McDonald, NJ Mendelsohn, JB Moeschler, B Moghaddam, G Neri, R Newbury-Ecob, RA Pagon, JA Phillips, JM Stoler, D Tilstra, CM Walsh Vockley, EH Zackai, TM Zadeh, Louise Brueton, GC Black, LG Biesecker

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