Literature DB >> 16454982

Three novel FOXL2 gene mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.

Siu-fong June Or1, Ming-for Tony Tong, Fai-man Ivan Lo, Tak-sum Stephen Lam.   

Abstract

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Year:  2006        PMID： 16454982

Source DB:  PubMed          Journal:  Chin Med J (Engl)        ISSN： 0366-6999            Impact factor:   2.628


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  3 in total

1.  FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.

Authors:  Juan Wang; Jinling Liu; Qingjiong Zhang
Journal:  Mol Vis       Date:  2007-01-26       Impact factor: 2.367

2.  FOXF2 is required for cochlear development in humans and mice.

Authors:  Guney Bademci; Clemer Abad; Armagan Incesulu; Fahed Elian; Azadeh Reyahi; Oscar Diaz-Horta; Filiz B Cengiz; Claire J Sineni; Serhat Seyhan; Emine Ikbal Atli; Hikmet Basmak; Selma Demir; Ali Moussavi Nik; Tim Footz; Shengru Guo; Duygu Duman; Suat Fitoz; Hakan Gurkan; Susan H Blanton; Michael A Walter; Peter Carlsson; Katherina Walz; Mustafa Tekin
Journal:  Hum Mol Genet       Date:  2019-04-15       Impact factor: 6.150

3.  Identification of the forkhead transcriptional factor 2 (FOXL2) gene mutations in four Chinese families with blepharophimosis syndrome.

Authors:  Li Zhang; Liming Wang; Ruifang Han; Lifang Guan; Baohong Fan; Mingmei Liu; Ming Ying; Hao Peng; Ningdong Li
Journal:  Mol Vis       Date:  2013-11-16       Impact factor: 2.367
  3 in total

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