A novel GLI3 mutation affecting the zinc finger domain leads to preaxial-postaxial polydactyly-syndactyly complex

Novel frame-shift mutations of GLI3 gene in non-syndromic postaxial polydactyly patients

(2014) Zhigang Wang et al.   CLINICA CHIMICA ACTA

New insights into genotype–phenotype correlation for GLI3 mutations

(2014) Florence Démurger et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Two Indian families with Greig cephalopolysyndactyly with non-syndromic phenotype

(2013) Sidharth Kumar Sethi et al.   EUROPEAN JOURNAL OF PEDIATRICS

Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations

(2010) Jennifer J. Johnston et al.   HUMAN MUTATION

Polydactyly and genes

(2010) Shubha R. Phadke et al.   INDIAN JOURNAL OF PEDIATRICS

The clinical atlas of Greig cephalopolysyndactyly syndrome

(2008) Katherine Balk et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The Greig cephalopolysyndactyly syndrome

(2008) Leslie G Biesecker   Orphanet Journal of Rare Diseases