A bibliometric overview of craniosynostosis research development.

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[2]  J. Goos,et al.  Genetic Causes of Craniosynostosis: An Update , 2018, Molecular Syndromology.

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[4]  A. Munnich,et al.  Mutations within or upstream of the basic helix–loop–helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome , 1999, European Journal of Human Genetics.

[5]  A. Wilkie.  Craniosynostosis: genes and mechanisms. , 1997, Human molecular genetics.

[6]  E. Green,et al.  Mutations in TWIST, a basic helix–loop–helix transcription factor, in Saethre-Chotzen syndrome , 1997, Nature Genetics.

[7]  E. Zackai,et al.  Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes , 1996, Nature Genetics.

[8]  W. Reardon,et al.  Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome , 1995, Nature Genetics.

[9]  W. Reardon,et al.  A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome , 1994, Nature Genetics.

[10]  Sue Malcolm,et al.  Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome , 1994, Nature Genetics.

[11]  E. Jabs,et al.  A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis , 1993, Cell.

[12]  A. Hockley,et al.  Craniosynostosis , 1993, The Lancet.

[13]  A. Hunter,et al.  Craniosynostosis. II. Coronal synostosis: its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactyly. , 1977, Teratology.

[14]  A. Hunter,et al.  Craniosynostosis. I. Sagittal synostosis: its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s). , 1976, Teratology.

[15]  P. Tessier.  [Total facial osteotomy. Crouzon's syndrome, Apert's syndrome: oxycephaly, scaphocephaly, turricephaly]. , 1967, Annales de chirurgie plastique.