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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

Bartsch, O., Schmidt, S., Richter, M., Morlot, S., Seemanová, E., Wiebe, G., et al. (2005). DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein-Taybi syndrome (RSTS) and in another patient with incomplete RSTS. Human Genetics, 117(5), 485-493.

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 Creators:
Bartsch, O., Author
Schmidt, S., Author
Richter, M., Author
Morlot, S., Author
Seemanová, E., Author
Wiebe, G.1, Author           
Rasi, S., Author
Affiliations:
1Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              

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Free keywords: CREB binding protein; Rubinstein-Taybi syndrome; small molecular mutations
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Language(s): eng - English
 Dates: 2005-09
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 281146
ISI: 000231325700008
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Title: Human Genetics
  Alternative Title : Hum. Genet.
Source Genre: Journal
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Publ. Info: -
Pages: - Volume / Issue: 117 (5) Sequence Number: - Start / End Page: 485 - 493 Identifier: ISSN: 0340-6717