Associated Papers
The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis.
Berry FB et al.
Human Molecular Genetics, 2005
Lymphoedema-distichiasis and FOXC2: unreported mutations, de novo mutation estimate, families without coding mutations.
Sholto-Douglas-Vernon C et al.
Human Genetics, 2005
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