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2293.
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Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations. [electronic resource] by
- 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, John M
- Grange, Dorothy K
- Guttmacher, Alan E
- Hannibal, Mark C
- Henn, Wolfram
- Hennekam, Raoul C 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, 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
Producer: 20050516
In:
American journal of human genetics vol. 76
Availability: No items available.
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