Literature DB >> 22605842

Crouzon syndrome.

Rekha Khandelwal1, Pulak Agrawal, Mohana Raja Majumdar.   

Abstract

Entities:  

Mesh：

Year:  2012        PMID： 22605842      PMCID： PMC3351648          DOI： 10.1136/bcr.05.2011.4196

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN： 1757-790X


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  1 in total

1.  Ophthalmic sequelae of Crouzon syndrome.

Authors:  Timothy L Gray; Theresa Casey; Dinesh Selva; Peter J Anderson; David J David
Journal:  Ophthalmology       Date:  2005-06       Impact factor: 12.079
  1 in total
  4 in total

1.  Crouzon syndrome in a fraternal twin: A case report and review of the literature.

Authors:  Xiao-Jing Li; Ji-Mei Su; Xiao-Wei Ye
Journal:  World J Clin Cases       Date:  2022-06-06       Impact factor: 1.534

2.  C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients.

Authors:  Ying Lin; Hongbin Gao; Siming Ai; Jacob V P Eswarakumar; Chuan Chen; Yi Zhu; Tao Li; Bingqian Liu; Xialin Liu; Lixia Luo; Hongye Jiang; Yonghao Li; Xiaoling Liang; Chenjin Jin; Xinhua Huang; Lin Lu
Journal:  Mol Med Rep       Date:  2017-08-14       Impact factor: 2.952

3.  FGFR2 mutations and associated clinical observations in two Chinese patients with Crouzon syndrome.

Authors:  Ying Lin; Hongbin Gao; Siming Ai; Jacob V P Eswarakumar; Yi Zhu; Chuan Chen; Tao Li; Bingqian Liu; Hongye Jiang; Yuhua Liu; Yonghao Li; Qingxiu Wu; Haichun Li; Xiaoling Liang; Chenjin Jin; Xinhua Huang; Lin Lu
Journal:  Mol Med Rep       Date:  2017-08-29       Impact factor: 2.952

Review 4.  Rare Genetic Syndromes and Oral Anomalies: A Review of the Literature and Case Series with a New Classification Proposal.

Authors:  Claudia Salerno; Valeria D'Avola; Luca Oberti; Elena Almonte; Elena Maria Bazzini; Gianluca Martino Tartaglia; Maria Grazia Cagetti
Journal:  Children (Basel)       Date:  2021-12-26
  4 in total

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