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Oxford University Press

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Identification of a Tbx1/Tbx2/Tbx3 genetic pathway governing pharyngeal and arterial pole morphogenesis

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ARX homeodomain mutations abolish DNA binding and lead to a loss of transcriptional repression

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Point Mutations in Human GLI3 Cause Greig Syndrome

By Wild Anja   Kalff-Suske Martha   Vortkamp Andrea   Bornholdt Dorothea   Kônig Rainer   Grzeschik Karl-Heinz  

Human Molecular Genetics, Vol. 6, Iss. 11, 1997-10 ,pp. : 1979-1984

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Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome

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