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

No abstract is available for this paper.

• Publication year

  2005

• Venue

  Human Genetics

• Publication date

  2005-07-14

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/s00439-005-1331-yPMID 16021471
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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