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                                       Details for article 16 of 24 found articles
 
 
  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.
Appeared in: The American journal of human genetics
Paging: Volume 76 (2005) nr. 4 pages 14 p.
Year: 2005
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 16 of 24 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands