Literature DB >> 15996217

Vertebral anomalies and cartilaginous tracheal sleeve in three patients with Pfeiffer syndrome carrying the S351C FGFR2 mutation.

M Gonzales, S Heuertz, J Martinovic, S Delahaye, A Bazin, P Loget, L Pasquier, M Le Merrer, J Bonaventure.   

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Year:  2005        PMID： 15996217     DOI： 10.1111/j.1399-0004.2005.00477.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  4 in total

Review 1.  Syndromic craniosynostosis, fibroblast growth factor receptor 2 (FGFR2) mutations, and sacrococcygeal eversion presenting as human tails.

Authors:  C Corbett Wilkinson; David K Manchester; Robert F Keating; Lawrence L Ketch; Ken R Winston
Journal:  Childs Nerv Syst       Date:  2012-06-04       Impact factor: 1.475

Review 2.  Tracheal Ring Formation.

Authors:  Dagmar Iber; Malte Mederacke
Journal:  Front Cell Dev Biol       Date:  2022-04-25

Review 3.  FGF/FGFR signaling in health and disease.

Authors:  Yangli Xie; Nan Su; Jing Yang; Qiaoyan Tan; Shuo Huang; Min Jin; Zhenhong Ni; Bin Zhang; Dali Zhang; Fengtao Luo; Hangang Chen; Xianding Sun; Jian Q Feng; Huabing Qi; Lin Chen
Journal:  Signal Transduct Target Ther       Date:  2020-09-02

4.  Tracheal cartilaginous sleeves in children with syndromic craniosynostosis.

Authors:  Tara L Wenger; John Dahl; Elizabeth J Bhoj; Anna Rosen; Donna McDonald-McGinn; Elaine Zackai; Ian Jacobs; Carrie L Heike; Anne Hing; Avni Santani; Andrew F Inglis; Kathleen C Y Sie; Michael Cunningham; Jonathan Perkins
Journal:  Genet Med       Date:  2016-05-26       Impact factor: 8.822
  4 in total

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