DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein–Taybi syndrome (RSTS) and in another patient with incomplete RSTS 期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein–Taybi syndrome (RSTS) and in another patient with incomplete RSTS

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.

作者姓名：	Bartsch O Schmidt S Richter M Morlot S Seemanová E Wiebe G Rasi S

摘要：
收稿时间：	2 February 2005
修稿时间：	16 April 2005
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