A bibliometric overview of craniosynostosis research development

Author:

Iping Rik,Cohen Adrian M.,Abdel Alim Tareq,van Veelen Marie-Lise C.,van de Peppel Jeroen,van Leeuwen Johannes P.T.M.,Joosten Koen F.M.,Mathijssen Irene M.J.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference16 articles.

1. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes;Bellus;Nat. Genet.,1996

2. Bibliometric analysis of the top 100 most cited articles on craniosynostosis;Elarjani;Childs Nerv. Syst.,2021

3. Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome;El Ghouzzi;Eur. J. Hum. Genet.,1999

4. Craniosynostosis;Foltz;J. Neurosurg.,1975

5. Clinical and surgical notes ON a series OF 78 cases OF craniosynostosis;Giuffre;Minerva Pediatr.,1975

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