Severe pancreas hypoplasia and multicystic renal dysplasia in two human fetuses carrying novel HNF1/MODY5 mutations

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Human Molecular Genetics, Vol. 15, Iss. 15, 2006-08 ,pp. : 2363-2375

Oxford University Press

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HNF1  / TCF2 mutations impair transactivation potential through altered co-regulator recruitment

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Human Molecular Genetics, Vol. 13, Iss. 24, 2004-12 ,pp. : 3139-3149

Oxford University Press

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MODY type 2 in Greig cephalopolysyndactyly syndrome (GCPS) as part of a contiguous gene deletion syndrome

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American Journal Of Medical Genetics Part A, Vol. 155, Iss. 10, 2011-10 ,pp. : 2469-2472

John Wiley & Sons Inc

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Isomers of the TCF1 gene encoding hepatocyte nuclear factor-1 alpha show differential expression in the pancreas and define the relationship between mutation position and clinical phenotype in monogenic diabetes

By Harries Lorna W.   Ellard Sian   Stride Amanda  

Human Molecular Genetics, Vol. 15, Iss. 14, 2006-07 ,pp. : 2216-2224

Oxford University Press

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TCF7L2 splice variants have distinct effects on -cell turnover and function

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Human Molecular Genetics, Vol. 20, Iss. 10, 2011-05 ,pp. : 1906-1915

Oxford University Press

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