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Human Molecular Genetics, Vol. 14, Iss. 18, 2005-09 ,pp. : 2619-2627

Oxford University Press

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Mutations in the Treacher Collins syndrome gene lead to mislocalization of the nucleolar protein treacle

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Towards a functional classification of pathogenic FOXL2 mutations using transactivation reporter systems

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Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1

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Human Molecular Genetics, Vol. 12, Iss. 22, 2003-11 ,pp. : 2993-3005

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Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation

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