Associated Papers
Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations.
Erickson RP et al.
Journal of Medical Genetics, 2001
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation.
De Baere E et al.
Human Molecular Genetics, 2001
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome.
Fang J et al.
American Journal of Human Genetics, 2000
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