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Oxford University Press

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A new sequence motif linking lissencephaly, Treacher Collins and oral–facial–digital type 1 syndromes, microtubule dynamics and cell migration

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Oxford University Press

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Kidney-specific inactivation of Ofd1 leads to renal cystic disease associated with upregulation of the mTOR pathway

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Human Molecular Genetics, Vol. 19, Iss. 14, 2010-07 ,pp. : 2792-2803

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Lowering of Pkd1 expression is sufficient to cause polycystic kidney disease

By Leeuwen Irma S. Lantinga-van  

Human Molecular Genetics, Vol. 13, Iss. 24, 2004-12 ,pp. : 3069-3077

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A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral–facial–digital type I syndrome

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Springer Publishing Company

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