Metopic and sagittal synostosis in Greig cephalopolysyndactyly syndrome: five cases with intragenic mutations or complete deletions of GLI3

Craniosynostosis: Diagnosis, Evaluation, and Management

Neurosurgery · 2001 · 559 citations

Sclerostin, Pathology, Craniosynostosis Syndromes +18

GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

Andrea Vortkamp, Manfred Gessler, Karl‐Heinz Grzeschik · Nature · 1991 · 544 citations

Gli3 Zinc-finger Gene, Developmental Biology, Mendelian Disorder +7

Prevalence and Complications of Single-Gene and Chromosomal Disorders in Craniosynostosis

Andrew O.M. Wilkie, Jo C. Byren, Jane A. Hurst et al. · PEDIATRICS · 2010 · 285 citations · Full text

Craniosynostosis. Diagnosis, Evaluation and Management

R. J. Hayward · Archives of Disease in Childhood · 1987 · 282 citations · Full text

Craniofacial Anomalies, Orbital Surgery, Surgery +4

Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations

Jennifer J. Johnston, Isabelle Olivos‐Glander, Christina Killoran et al. · The American Journal of Human Genetics · 2005 · 276 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +10