引用本文: | Bartsch O,Schmidt S,Richter M,Morlot S,Seemanová E,Wiebe G,Rasi S.DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein–Taybi syndrome (RSTS) and in another patient with incomplete RSTS[J].Human genetics,2005,117(5):485-493. |