Authors:
Giglio, Sabrina
Calvari, Vladimiro
Gregato, Giuliana
Gimelli, Giorgio
Camanini, Silvia
Giorda, Roberto
Ragusa, Angela
Guerneri, Silvana
Selicorni, Angelo
Stumm, Marcus
Tonnies, Holger
Ventura, Mario
Zollino, Marcella
Neri, Giovanni
Barber, John
Wieczorek, Dagmar
Rocchi, Mariano
Zuffardi, Orsetta
Citation: Giglio, Sabrina et al., Heterozygous Submicroscopic Inversions Involving Olfactory Receptor.Gene Clusters Mediate the Recurrent t(4;8)(p16;p23) Translocation, American journal of human genetics , 71(2), 2002, pp. 276-285
Authors:
Zollino, Marcello
Lecce, Rossetta
Fischetto, Rita
Murdolo, Marina
Favarelli, Francesca
Selicorni, Angelo
Buttè, Cinzia
Memo, Luigi
Capovilla, Giuseppe
Neri, Giovanni
Citation: Zollino, Marcello et al., Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region, WHSCR-2, American journal of human genetics , 72(3), 2003, pp. 590-597
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