Literature DB >> 9843059

Nonpenetrance in FGFR3-associated coronal synostosis syndrome.

N H Robin, J A Scott, A R Cohen, J A Goldstein.   

Abstract

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Year:  1998        PMID： 9843059

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  4 in total

Review 1.  Epilepsy in Muenke syndrome: FGFR3-related craniosynostosis.

Authors:  Nneamaka B Agochukwu; Benjamin D Solomon; Andrea L Gropman; Maximilian Muenke
Journal:  Pediatr Neurol       Date:  2012-11       Impact factor: 3.372

2.  Paternal origin of FGFR3 mutations in Muenke-type craniosynostosis.

Authors:  Sahan V Rannan-Eliya; Indira B Taylor; I Marieke De Heer; Ans M W Van Den Ouweland; Steven A Wall; Andrew O M Wilkie
Journal:  Hum Genet       Date:  2004-07-07       Impact factor: 4.132

3.  Muenke syndrome.

Authors:  G Sabatino; F Di Rocco; G Zampino; G Tamburrini; M Caldarelli; C Di Rocco
Journal:  Childs Nerv Syst       Date:  2004-02-10       Impact factor: 1.475

4.  Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.

Authors:  J Hughes; N C Nevin; P J Morrison
Journal:  Ulster Med J       Date:  2001-05
  4 in total

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