Loss of CBP acetyltransferase activity by PHD finger mutations in Rubinstein–Taybi syndrome

By Kalkhoven Eric  

Human Molecular Genetics, Vol. 12, Iss. 4, 2003-02 ,pp. : 441-450

Oxford University Press

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Expanding the phenotypic spectrum in EP300‐related Rubinstein–Taybi syndrome

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 5, 2015-05 ,pp. : 1111-1116

John Wiley & Sons Inc

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Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein–Taybi syndrome

By Bartsch Oliver   Rasi Sasan   Delicado Alicia   Dyack Sarah   Neumann Luitgard   Seemanová Eva   Volleth Marianne   Haaf Thomas   Kalscheuer Vera  

Human Genetics, Vol. 120, Iss. 2, 2006-09 ,pp. : 179-186

Springer Publishing Company

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Truncated CBP protein leads to classical Rubinstein–Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism

By Yamamura K-i.  

Human Molecular Genetics, Vol. 8, Iss. 3, 1999-03 ,pp. : 387-396

Oxford University Press

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Defect of histone acetyltransferase activity of the nuclear transcriptional coactivator CBP in Rubinstein–Taybi syndrome

By Rosenfeld M.G.  

Human Molecular Genetics, Vol. 10, Iss. 10, 2001-05 ,pp. : 1071-1076

Oxford University Press

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