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 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.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference49 articles.

1. Greig cephalopolysyndactyly: report of 13 affected individuals in three families;Baraitser;Clin Genet,1983

2. Interstitial deletion of the short arm of chromosome 7 without craniosynostosis;Bianchi;Clin Genet,1981

3. Strike three for GLI3;Biesecker;Nat Genet,1997

4. Pallister-Hall syndrome;Biesecker;GeneReviews at GeneTests,2003

5. Greig cephalopolysyndactyly syndrome;Biesecker;GeneReviews at GeneTests,2004

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