Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations

Authors	J.J. Johnston I. Olivos-Glander C. Killoran E. Elson J.T. Turner K.F. Peters M.H. Abbott D.J. Aughton A.S. Aylsworth M.J. Bamshad C. Booth C.J. Curry A. David M.B. Dinulos D.B. Flannery M.A. Fox J.M. Graham D.K. Grange A.E. Guttmacher M.C. Hannibal W. Henn R.C.M. Hennekam L.B. Holmes H.E. Hoyme K.A. Leppig A.E. Lin P. MacLeod D.K. Manchester C. Marcelis L. Mazzanti E. McCann M.T. McDonald N.J. Mendelsohn J.B. Moeschler B. Moghaddam G. Neri R. Newbury-Ecob R.A. Pagon J.A. Philips III L.S. Sadler J.M. Stoler D. Tilstra C.M. Walsh Vockley E.H. Zackai T.M. Zadeh L. Brueton G.C.M. Black L.G. Biesecker
Publication date	2005
Journal	American Journal of Human Genetics
Volume \| Issue number	76 \| 4
Pages (from-to)	609-622
Organisations	Faculty of Medicine (AMC-UvA)
Document type	Article
Note	Bethesda MD. © Chicago UP
Published at	https://doi.org/10.1086/429346 (Final published version)
Downloads	207975y.pdf
Permalink to this page

Back

UvA-DARE