FOXC2truncating mutation in distichiasis, lymphedema, and cleft palate
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2002.620608.x/fullpdf
Reference8 articles.
1. Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene;Bell;Hum Genet,2001
2. Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24;Brice;J Med Genet,2002
3. A gene for lymphedema-distichiasis maps to 16q24.3;Mangion;Am J Hum Genet,1999
4. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome;Fang;Am J Hum Genet,2000
5. Clustered arrangement of winged helix genes fkh-6 and MFH-1: possible implications for mesoderm development;Kaestner;Development,1996
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